As I was typing this, we have been hit with a plume of type Burnt Electronics/Fungal. Following is the event profile:
~11 am Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity (11:10 am): 9+, Rising
The vast majority of people still have no clue how profoundly the spraying affects their health and mood. I have witnessed this correlation between health/mood and spraying intensity for years because I smell and taste it in the air enabling me to know when people are being directly affected.
You can't simply look in the sky at trails and know how bad the air is. Although this used to be true to some degree, over a decade ago, they began using short, non-persistent trails that dissipate nearly immediately and they spray these at low and high altitudes. These plumes are just at potent (often more) than the persistent plumes, so the correlation between visible trails and air quality no longer exists.
The spraying program is more complex than more realize. There are a myriad of types, plus, there are clearly at least 2 separate programs that have no direct relationship to each other. One program is clearly associated with populations and the other is associated with weather systems. The program associated with populations is temporally related to holidays, public events, and wake/sleep patterns. The program associated with weather is temporally related to weather systems. So like most things in life, the spray program is more complex than most people realize.
11:22 am
The intensity of the previous wide-spectrum plume is now 8.5+ and falling.
The intensity of the previous Burnt type plume is now 9.5+ and may be peaking now.
When first used, the Burnt type plumes were always very brief. Now, they last much longer than when they first appeared, which was just this year. They are a brand new type.
The previous plume is being layered keeping the intensity high for long-periods of time. Something they didn't do until the past few years.
Intensity as I type this (2:13 pm) is 9.5 and steady. This is horrible and nearly unbreathable inducing nausea, vertigo, fatigue, pain, heart issues, and much more. This is like torture for us. It is incredibly bad.
This is poison folks. More people smell and taste it in the air than ever before. I hope all who do speak out daily against this epic, history, and unequalled crime against humanity.
3:34 pm
The previous plume slowly tapered off reaching intensity 8.
Then, at about 3:20 pm, we were hit with another very strong wide-spectrum plume. This one also it dominated by the (likely) plastic-containing Model Cement/Burnt Plastic type.
The previous plume peaked above 10, then slowly tapered off reaching intensity 8 just like earlier this afternoon.
At about 5 pm, we were hit with another very strong wide-spectrum plume. This one also it dominated by the (likely) plastic-containing Model Cement/Burnt Plastic type.
~6:10 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.25, Rising
7:32 pm
At about 7 pm, we were hit with another very strong wide-spectrum plume. This one also it dominated by the (likely) plastic-containing Model Cement/Burnt Plastic type.
You have heard about PFAS "forever plastics" saturating the environment. Now you know where it's coming from. It's what you breath.
The previous wide-spectrum plume is being layered and is at intensity 9 as I type this. They are really hitting us hard.
We have now been hit with a Burnt type plume. Following is the event profile:
~8 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75, Rising
10:22 pm
We had a little break from about 9 pm until 10:18 pm. It wasn't much of a break because intensity only dropped to 7.75, which is not good.
At 10:18 pm we were hit with a wide-spectrum plume that rose very quickly and is now already at intensity 9.75 as I type this. This is absolutely horrible.
Now, as I type this, intensity has already risen to 10, but now we are also being hit with a Burnt type plume. There are no words.
People wonder why so many are sick today. This is no mystery to us at all.
~10:24 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75, Rising
12:26 am
At 11:50 pm we were hit with a light "layering" plume that nudged intensity up slowly, but at about 12:20 pm we were hit with a typical wide-spectrum plume. Intensity is now rising quickly.
We have also been hit with a Burnt type plume. No surprise.
~12:23 am Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.25, Rising
What a time we live in. Where are you America? ...World?
1:51 am
They are layering the Chalky-Bitter-Pharma type in the air. This is the type that rapidly depletes magnesium (in some more than others) and could induce heart attacks. They often layer this type for 4 to 8 hours at a time. They are doing it again tonight.
Following is a snapshot of the current condition of the air:
They layered the previous plume all afternoon and it continues at I type this at the current intensity of 9.5.
~11:15 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 8.75+
~12:15 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 8.75
3:32 pm
And so it continues. The previous wide-spectrum plume continues to be in the air at a horrible, nearly-unbreathable intensity of 9.25 as I type this. The type profile of the mixture is the same as it has been all day:
At 4:45 pm we were also hit with a Burnt type plume:
~4:45 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 8.5
6:47 pm
We are now being hit with wide-spectrum plume. Following is the event profile:
~6:35 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Chalky-Bitter-Pharma - Dominant - Inflammatory - Mercury Intensity Delta: Medium-Fast Current Intensity: 9.25, Rising
7:24 pm
They are layering the previous plume keeping intensity high.
Intensity of the previous plume is now 10. This has been a brutal day of spraying.
8:31 pm
From about 7:50 pm until 8:18 pm we had a little "break". Intensity fell to 7.25+ during this brief time.
At about 8:18 pm we were hit with a wide-spectrum plume. This was a partial hit that rose very quickly and is now already declining. The Model Cement/Burnt Plastic type has returned as the dominant plume.
We are how being hit with a plume of type Burnt Electronics/Fungal:
~8:50 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75+, Rising
11:51 pm
We had our evening break from about 9:50 pm until 10:30 pm. Intensity dropped to 7.5-. It felt great. Nearly all of the inflammation and pain disappeared as it does at this intensity. I really want this madness to stop. I have suffered su much.
At about 10:30 pm we were hit with a light ("layering") plume that raised intensity 7.75 with the Chalky-Bitter-Pharma type being dominant.
At about 11:45 pm we were hit with a typical plume with the following profile:
At 7 am we were hit with a wide-spectrum plume that peaked at intensity 9.5.
At 11 am we were hit with a wide-spectrum plume.
At 12 n we were hit with a wide spectrum plume.
From 12 n on we were layered. They pushed intensity up to 8.5 and kept it there.
Without breaks, at 9 pm and 9:45 pm we were hit with 2 more wide-spectrum plumes that both peaked at 9.25.
December 28 - The Daily Spraying Log
No plumes in the am.
At 1:20 pm we were hit with a wide-spectrum plume that peaked at intensity 10.
At 2:50 pm we were hit with a wide-spectrum plume dominated by the inflammatory type.
After this plume cleared, intensity fell to an ambient intensity of 7.5 until 5:25 pm.
At 5:25 pm we were hit with a wide-spectrum plume that peaked at intensity 10.
At 8 pm we were hit with a wide-spectrum plume that peaked at intensity 10.
At 9:10 pm we were hit with a wide-spectrum plume dominated by the horrific Chalky-Bitter-Pharma type.
At 12:39 am we were hit with a wide-spectrum plume.
At 1:45 am we were hit with a Burnt type plume that peaked at intensity 8.5+.
December 27 - The Daily Spraying Log
This was another remarkable day. We had not discrete plumes today. Are the pilots getting a vacation?
Intensity was at 7.75+ all day with the typical wide-spectrum mix of poisons.
Intensity fell a little during our typical evening break between 8:30 pm and 10:30 pm.
At 10:30 pm we were hit with a wide-spectrum plume that peaked at intensity 10.
December 26 - The Daily Spraying Log
This was a remarkable day unlike any other I have experienced since spraying began in our area in 2005.
Listen carefully: We had no discrete plumes today. None. Zero.
Intensity was layered at a median intensity throughout the day between 7.75 and 8+: not mild but not brutal. The type of poison being layered on us was dominated by the Chalky-Bitter-Pharma type.
We were hit with our first plume at 10:50 pm; a wide-spectrum plume.
We were hit at 3 am with a wide-spectrum plume that peaked at intensity 10. The dominant plume type was the inflammatory type.
December 25 - The Daily Spraying Log
A brief look at the spraying activity for the day. I was in Bangor much of the day so this applies to that location.
7:50 am - Hit with a wide-spectrum plume. They layered the entire day.
By 10 am intensity was 8 and layering continued but the formula changed to include the following types in order from strongest to weakest:
Not a bad night of poisoning, relatively speaking. Intensity through the night ranged between 7.5 and 7.75-, so it was pretty steady and milder than usual, but by no means clear. At this intensity, it still has health effects on us, they are just not at pronounced. Poison is still poison.
The only plume we have had today so far hit us at about 6 am. Intensity rose to 9 and then subsided within 40 minutes back to ambient levels.
That's it so far.
Are the pilots and other supporting getting a holiday this year?
Whatever the reason, I'm thankful for the current condition of the air, which is a poison-but-tolerable 7.5 intensity. This makes us feel a little tired an fatigued, and produces a little inflammation, but it's tolerable and enables us to remain functional, although I suspect we will be having some plumes this afternoon and evening. We'll see.
I will be reporting it all in this log.
12:56 pm
Well that didn't take long. Just a few minutes after making the previous entry, we have been hit with a wide-spectrum plume.
Zembrin® (Sceletium tortuosum extract) is a standardized patented extract of Sceletium tortuosum, a South African plant that has been used for centuries for its medicinal benefits, as well as its mood-enhancing and anti-anxiety properties. Sceletium tortuosum contains active ingredients known as alkaloids that have been shown to selectively inhibit serotonin reuptake. Serotonin is a molecule (a chemical "messenger" or neurotransmitter) that plays an important role in modulating mood and other behaviors such as sleep and perception of pain. Serotonin can also suppress elevated activity in the amygdala (the region of the brain involved with emotions, emotional behavior and motivation), which has been correlated with anxiety and fear response in animal and clinical studies. Inhibiting serotonin reuptake, which keeps levels of serotonin higher, is reported to be one of the pharmacological actions by which Sceletium tortuosum can affect mood and anxiety states, as well as sleep quality. Incidentally, serotonin reuptake inhibitors are among the most widely prescribed compounds for treatment of anxiety disorders and depression. Zembrin® has been patented for use as a serotonin-uptake inhibitor in formulas designed to help manage anxiety and depression. In a recent randomized double-blind, placebo-controlled study, participants taking Zembrin® reported positive effects from taking the patented extract, including improvement in sleep and in handling stress. In another double-blind, placebo-controlled, cross-over study, a single dose of Zembrin® was shown to reduce anxiety-related brain activity in healthy participants.4-16
L-Theanine, a naturally occurring non-protein amino acid found in green tea leaves, has demonstrated diverse physiological activity, including lowering blood pressure, reducing anxiety and stress, promoting relaxation, and improving mood and brain function (e.g. concentration and learning ability). L-theanine has been shown to cross the blood-brain barrier, causing significant increases in brain concentrations of the neurotransmitters serotonin and dopamine. Serotonin is involved in behavior such as mood and sleep, while dopamine plays an important role in brain activity and the functioning of the central nervous system. L-Theanine, which has a direct effect on the brain, has also been shown to relax the mind without causing drowsiness. L-Theanine stimulates the brain’s production of alpha waves, thus enabling a person to achieve a relaxed but alert mental state. In addition, l-Theanine has been shown to improve mood in adults by reducing anxiety and tension resulting from psychological stress.17-23
Thiamin (B1, mononitrate) - Thiamin, also known as vitamin B1, plays an important role in glucose energy utilization, particularly in the central nervous system. Thiamin is also essential for healthy brain and nervous system function and has been termed the "morale vitamin" as a result of its beneficial effect on mental attitude. Thiamin deficiency is associated with depressive behaviors, as well as aggressiveness, confusion and memory impairment. Research suggests that thiamin has antidepressant and anxiolytic (ability to reduce anxiety, agitation or tension) effects and double-blind studies have shown an association between improved thiamin status and elevated mood. In one study of 120 young adult females, improved thiamin status correlated with reports of participants being more clear-headed, composed and energetic—these results were demonstrated in participants whose thiamin status was "adequate" according to traditional standards.24-33
Magnesium (citrate) - Magnesium, one of the most essential minerals in the body, plays an important role in brain biochemistry. Research indicates that inadequate brain magnesium levels are correlated with reduced serotonin levels and anxiety-related behavior, as well as treatment-resistant depression. In fact, magnesium deficiency is associated with a number of psychiatric symptoms, including anxiety, apathy, depression, fatigue, irritability and weakness. Magnesium depletion has been proven to cause depression and anxiety behavior in animals. In addition, acute emotional stress and stressful activities increase magnesium excretion, thus reducing intracellular magnesium levels in humans. Numerous pre-clinical and clinical studies have confirmed the potential benefits of magnesium for the treatment of anxiety and depression and have demonstrated the safety of magnesium supplementation.3,34-41
Zinc (gluconate) - Zinc is an essential trace mineral that contributes to the normal absorption and action of vitamins, especially the B-complex vitamins. Zinc is also essential for normal functioning of the brain and central nervous system. Evidence suggests that zinc levels decline following physical and mental stress. Zinc deficiency has been shown to induce depression and anxiety-like behaviors and mood disorders. A study of patients with generalized anxiety disorder found significantly decreased serum zinc levels among patients when compared to healthy volunteers. Likewise, lower zinc levels were associated with higher anxiety and conduct problems among students with ADHD (Attention Deficit Hyperactivity Disorder) symptoms. Furthermore, several studies have demonstrated zinc’s antidepressant and anxiolytic activity in humans. Studies have shown that symptom severity in individuals with anxiety (both with and without secondary depression) improved significantly following zinc supplementation.1,25,28,32,42-47
References: 1Russo, A.J. "Decreased zinc and increased copper in individuals with anxiety." Nutrition and Metabolic Insights; 2011, 4:1-5. 2Abumaria, N., et. al. "Effects of elevation of brain magnesium on fear conditioning, fear extinction, and synaptic plasticity in the infralimbic prefrontal cortex and lateral amygdala." The Journal of Neuroscience; 2011, 31(42):14871-14881. 3Laarakker, M.C., et. al. "Behavioral characterization of A/J and C57BL/6J mice using a multidimensional test: association between blood plasma and brain magnesium-ion concentration with anxiety." Physiology & Behavior; 2011, 102(2):205-219. 4Harvey, A.L., et. al. "Pharmacological actions of the South African medicinal and functional food plant Sceletium tortuosum and its principal alkaloids." Journal of Ethnopharmacology; 2011, 137(3):1124-1129. 5Gericke, N., Viljoen, A.M. "Sceletium—a review update." Journal of Ethnopharmacology; 2008, 119(3):653–663. 6Shikanga, E.A., et. al. "A novel approach in herbal quality control using hyperspectral imaging: discriminating between Sceletium tortuosum and Sceletium crassicaule." Phytochemical Analysis; 2013, 24(6):550-555. 7Patnala, S., Kanfer, I. "Investigations of the phytochemical content of Sceletium tortuosum following the preparation of "Kougoed" by fermentation of plant material." Journal of Ethnopharmacology; 2009, 121(1):86-91. 8—. "HPLC analysis of mesembrine-type alkaloids in Sceletium plant material used as an African traditional medicine." Journal of Pharmacy and Pharmaceutical Sciences; 2010, 13(4):558-570. 9—. "A capillary zone electrophoresis method for the assay and quality control of mesembrine in Sceletium tablets." Journal of Pharmaceutical and Biomedical Analysis; 2008, 48(2):440-446. 10Stafford, G.I., et. al. "Review on plants with CNS-effects used in traditional South African medicine against mental diseases." Journal of Ethnopharmacology; 2008, 119(3):513-537. 11Terburg, D., et. al. "Acute effects of Sceletium tortuosum (Zembrin), a dual 5-HT reuptake and PDE4 inhibitor, in the human amygdala and its connection to the hypothalamus." Neuropsychopharmacology; 2013, 38(13):2708-2716. 12Donaldson, Z.R., et. al. "Genetic approaches for understanding the role of serotonin receptors in mood and behavior." Current Opinion in Neurobiology; 2013, 23(3):399-406. 13Curran, K.P., Chalasani, S.H. "Serotonin circuits and anxiety: what can invertebrates teach us?" Invertebrate Neuroscience; 2012, 12(2):81-92. 14Yamauchi, M., et. al. [Role of the serotonergic nervous system in anxiety disorders and the anxiolytic mechanism of selective serotonin reuptake inhibitors]. Nihon Shinkei Seishin Yakurigaku Zasshi; 2006, 26(5-6):193-198. 15Mandrioli, R., et. al. "Selective serotonin reuptake inhibitors (SSRIs): therapeutic drug monitoring and pharmacological interactions." Current Medicinal Chemistry; 2012, 19(12):1846-1863. 16Nell, H., et. al. "A randomized, double-blind, parallel-group, placebo-controlled trial of Extract Sceletium tortuosum (Zembrin) in healthy adults." Journal of Alternative and Complementary Medicine; 2013, 19(11):898-904. 17Desai, M.J. & Armstrong, D.W. et. al "Analysis of derivatized and underivatized theanine enantiomers by high-performance liquid chromatography/atmospheric pressure ionization-mass spectrometry." Rapid Communications in Mass Spectrometry; 2004, 18(3):251-256. 18Lu, K., et. al. "The acute effects of L-theanine in comparison with alprazolam on anticipatory anxiety in humans." Human Psychopharmacology; 2004, 19(7):457-465. 19Cooper, R., et. al. "Medicinal benefits of green tea: part I. Review of noncancer health benefits." Journal of Alternative & Complementary Medicine; 2005, 11(3):521-528. 20Vuong, Q.V., et. al. "L-Theanine: properties, synthesis and isolation from tea." Journal of the Science of Food and Agriculture; 2011, 91(11):1931-1939. 21Nobre, A.C., et. al. "L-theanine, a natural constituent in tea, and its effect on mental state." Asia Pacific Journal of Clinical Nutrition; 2008, 17 Suppl 1:167-168. 22Scheid, L., et. al. "Kinetics of L-theanine uptake and metabolism in healthy participants are comparable after ingestion of L-theanine via capsules and green tea." The Journal of Nutrition; 2012, 142(12):2091-2096. 23Yoto, A., et. al. "Effects of L-theanine or caffeine intake on changes in blood pressure under physical and psychological stresses." Journal of Physiological Anthropology; 2012, 31:28. 24Kelly ND, G.S. "Nutritional and Botanical Interventions to Assist with the Adaptation to Stress." Alternative Medicine Review; 1999, 4(4):249-265. 25Dunne, L.J. Nutrition Almanac, 3rd Ed. NY, NY: McGraw-Hill Publishing Co.; 1990. 26Benton, D. & Donohoe, R.T. "The effects of nutrients on mood." Public Health Nutrition; 1999, 2(3A):403-409. 27Benton, D., et. al. "Thiamine supplementation mood and cognitive functioning." Psychopharmacology (Berl); 1997, 129(1):66-71. 28Lieberman PhD, S. & Bruning, N. The Real Vitamin & Mineral Book, 2nd Ed. Avery Publ.; 1997. 29"Thiamine." Alternative Medicine Review; 2003, 8(1):59-62. 30Guilland, J.C. [Vitamin B1 (thiamine)]. La Revue du Practicien; 2013, 63(8):1074-1075,1077-1078. 31Bourre, J.M. "Effects of nutrients (in food) on the structure and function of the nervous system: update on dietary requirements for brain. Part 1: micronutrients." The Journal of Nutrition, Health & Aging; 2006, 10(5):377-385. 32Nikseresht, S., et. al. "Acute administration of Zn, Mg, and thiamine improves postpartum depression conditions in mice." Archives of Iranian Medicine; 2012, 15(5):306-311. 33Zhang, G., et. al. "Thiamine nutritional status and depressive symptoms are inversely associated among older Chinese adults." The Journal of Nutrition; 2013, 143(1):53-58. 34Serefko, A., et. al. "Magnesium in depression." Pharmacological Reports; 2013, 65(3):547-554. 35Eby 3rd, G.A., Eby, K.L. "Magnesium for treatment-resistant depression: a review and hypothesis." Medical Hypotheses; 2010, 74(4):649-660. 36Murck, H. "Ketamine, magnesium and major depression--from pharmacology to pathophysiology and back." Journal of Psychiatric Research; 2013, 47(7):955-965. 37Cubala, W.J., et. al. "Magnesium in drug-naïve patients with a short-duration, first episode of major depressive disorder: impact on psychopathological features." Magnesium Research; 2013, 26(4):192-198. 38Sartori, S.B., et. al. "Magnesium deficiency induces anxiety and HPA axis dysregulation: modulation by therapeutic drug treatment." Neuropharmacology; 2012, 62(1):304-312. 39Takase, B., et. al. "Effect of chronic stress and sleep deprivation on both flow-mediated dilation in the brachial artery and the intracellular magnesium level in humans." Clinical Cardiology; 2004, 27(4):223-227. 40Grases, G., et. al. "Anxiety and stress among science students. Study of calcium and magnesium alterations." Magnesium Research; 2006, 19(2):102-106. 41Forsyth, A.K., et. al. "Nutrition status of primary care patients with depression and anxiety." Australian Journal of Primary Health; 2012, 18(2):172-176. 42Pizzorno, J & Murray, M. A Textbook of Natural Medicine, 2nd ed. London: Churchill Livingstone, 1999. 43King, J.C. "Zinc: an essential but elusive nutrient." The American Journal of Clinical Nutrition; 2011, 94(2):679S-684S. 44Cope, E.C., Levenson, C.W. "Role of zinc in the development and treatment of mood disorders." Current Opinion in Clinical Nutrition and Metabolic Care; 2010, 13(6):685-689. 45Islam, M.R., et. al. "Comparative analysis of serum zinc, copper, manganese, iron, calcium, and magnesium level and complexity of interelement relations in generalized anxiety disorder patients." Biological Trace Element Research; 2013, 154(1):21-27. 46Oner, O., et. al. "Effects of zinc and ferritin levels on parent and teacher reported symptom scores in attention deficit hyperactivity disorder." Child Psychiatry and Human Development; 2010, 41(4):441-447. 47Russo, A.J. "Analysis of plasma zinc and copper concentration, and perceived symptoms, in individuals with depression, post zinc and anti-oxidant therapy." Nutrition and Metabolic Insights; 2011, 4:19-27.
The Log Continued
3:14 pm
Since the previous plume at 12:45 pm, they have been layering keeping intensity at 9.75+, nearly unbreathable.
One very significant thing has changed in the layered plumes:
The Mercury component is now dominant. We are having horrible mercury symptoms.
This is absolutely no surprise as they usually do this during times of public gathering. Mercury alters hormones and enzymes inducing fear and a host of negative emotions. See The Emotional Effects of Mercury
They love to concentrate mercury during social times, likely to cause division because this is what mercury ultimately does. It even causes division within one's self as it is a known cause of schizophrenia.
We have been hit with another plume before the previous plume has time to dissipate. So maybe now the light-ish spraying that we have had for the past 3 days is ending. We'll see.
They are now making the Inflammatory, Mercury, and Barium types dominant:
~7 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Inflammatory - Mercury - Barium Intensity Delta: Medium-Fast Current Intensity: 10
11:27 pm
We have been hit with a wide-spectrum plume. This plume is a conventional wide-spectrum plume containing the most common components.
As I type this, we are having our nightly "break". Since about 9:45 pm, intensity has been 7.5-, and it feel somewhat better at this level. Most of the inflammation and pain goes away, so at least there's that.
We have been hit with a number of plumes today. There was only a little layering between plumes this morning. Intensity fell to ambient levels between the rest of the plumes, like it did in the old days (last year and before).
Between this plume and the next, they layered continuously raising intenisty up until the next plume hit us. The next plume peaked at 10, so this was a very rough day to start the day.
Between this plume and the next, intensity fell to near-ambient (7.5+), which was nice. We didn't get hit with our usual 11:30 am and 1 pm plumes. Average spray intensity has dropped the past 3 days, and I wonder if this is related to the holiday.
~8:15 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 8.25, This was short-lived. It was clearly a partial hit.
They layered the remainder of the morning and afternoon with short, non-persistent (weaker) "layering plumes" to keep intensity elevated throughout the morning and afternoon. The type profile they continuously sprayed us with follows:
- Chalky-Bitter-Pharma - Dominant - Model Cement/Burnt Plastic - See Microplastics - Inflammatory - Mercury Continuous Intensity: 8.25 - This is enough to make you feel tired, weak, achy, unfocused, and much more. The dominant Chalky type steals magnesium from the body exactly as venom peptides do. Based on the precisely-aligned symptom set, I would say it's likely this type contains venom peptides or or a venom peptide plasmid such as was used in the so-called Covid vaccine. I will post videos below explaining this position later today. Do not discount this idea. When you view the available data, it is a strong position.
As I was making this log entry, we were hit with a burnt type plume. Following is the type profile:
~3 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.5, Rising
11:09 pm
It has been an interesting afternoon and evening. Makes me worried about what the night will bring.
After the 2 previous plumes (2:50 pm and 3 pm) hit us, they layered all afternoon and early evening with the following components. These are the same components they used to layer all morning. The only difference is that they also layered the Burnt type, which is not something they usually do, but it has become more common these day. Following is the mix we breathed between about 4 pm and 7 pm:
The intensity of the mix was fairly constant at 8.25, just like this morning.
At about 7 pm intensity began to drop and we had our evening "break". Intensity fell to 7.5- which provided relief of most symptoms.
The break ended at about 10:10 pm when intensity began to rise slowly to 8+. The mix is the same as shown above. In the past 10 minutes, intensity has fallen back to 7.5 where it remains as I type this (11:22 pm).
So, this day had a long stretch without discrete plumes (since 3 pm), only layering. Is this an early holiday break for the pilots and personnel?
With the chaos from the windstorm, I'm late getting this log out, but here it is.
Overnight was typical with intensity between 7.5 and 7.75 throughout the night.
Following is the list of plumes we wee hit with.
3:30 pm - Wide-spectrum plume, peak intensity: 10
4:09 pm - Burnt-type plume
They layered all afternoon beginning with the 3:30 pm plume. The kept intensity between 8.5 and 9. Not a good day.
Between about 9 pm and 11 pm we had our nightly break. Intensity fell to 7.5-. It was a very welcomed relief from all the pain and suffering we endure daily from the poisons they are spraying.
11 pm we were hit with an odd plume. it was dominated by the TYPE III Biologic type and the Chalky-Bitter-Pharma type. The TYPE III Biologics make you feel like you have the flu except you have no fever or respiratory issues. Your body just hurts all over. A friend told me it makes him feel like he's been tossed into a dryer. That is a great description. I completely get it.
From 1 am (12/22) onward, we had ambient intensity in the air at about 7.75 all night, until morning.
A typical night of spraying with wide-spectrum toxins in the air throughout the night at intensity 7.75-. Intensity was very steady until we were hit with a powerful plume this morning. Following is the event profile:
They have been layering this plume ever since 11 am keeping the intensity at a very painful 8.75+.
At about 1:30 pm we were hit again with the same type of plume. intensity rose to 10 where it continues 45 minutes later as I type this. Following is the event profile:
The intensity of the previous plume is now 10 (of 10). This is really brutal.
5:53 pm
We are now being hit with a Burnt type plume.
~5:45 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.5, Rising
9:23 pm
They continued layering plumes for hours. The air didn't begin clearing until about 8:30 pm.
I have written before about layering and how they can migrate types gradually as they layer in new plumes. After the previous wide spectrum plume, they quickly began layering in the Barium type, which quickly became dominant. The mercury type became a close third. It was truly a brutal afternoon of spraying with intensity between 9 and 10 the entire time.
By about 9 pm intensity had dropped to 7.5-, so we are now in our nightly break.
What a time we live in.
12:54 am (12/21)
We have been hit with 3 plumes since the previous log entry.
The 2 wide-spectrum plumes were different in that they did not have the usual Model Cement/Burnt Plastic type as the dominant component. Instead, they were dominated by the Chalky type. This is the type that clearly interferes with magnesium metabolism and can cause heart problems, among other things.
The Burnt type plume was typical.
The event profiles are below:
11:30 pm (12/21) Event: Hit with wide-spectrum plume. This hit at exactly 11:30 pm to the minute. This is the usual time we get hit most nights. This is the usual time we get hit most nights, but it's not normally right to the exact minute. This and the next plume hit us at exactly 11:30 pm and 12 m. Components (strongest to weakest): - Chalky-Bitter-Pharma - Dominant - Inflammatory - Mercury Intensity Delta: Medium-Fast Peak Intensity: 9.75+ (of 10)
12 m (12/21) Event: Hit with wide-spectrum plume. This hit at exactly 12 midnight to the minute. Components (strongest to weakest): - Chalky-Bitter-Pharma - Dominant - Inflammatory - Mercury Intensity Delta: Medium-Fast Peak Intensity: 9.5+ (of 10)
~12:30 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peal Intensity: 8.5+
December 19 - The Daily Spraying Log AI Tests Apollo Photos - Steering Hurricanes: An Old Technology - Microwaved Food - Stopping Heart Attacks
We had a horrible storm in the north east which came from the south. It has affected many people. With it came intense spraying of a different kind, a change that only those who smell and/or taste the fallout can detect.
Those who keep up with available information know that there are at least 2 active spraying programs. One program is clearly associated with weather. The other with simply distributing known poisons as far and wide as possible. The spray patterns we see clearly model these 2 purposes.
Having said that, we have had a bad night of spraying following this near-hurricane strength storm. They have been layering all night keeping intensity high. Intensity has been kept between 9 and 9.5 through the night. Following is the mix that has been in the air, and is still in the air as I type this:
Clove bud essential oil contains the phenol eugenol, a powerful anti-inflammatory agent that inhibits prostaglandin E (PGE) synthesis. Research shows that eugenol is strongly anesthetic—supporting its traditional use as an analgesic dentrifice for toothache—and antiseptic against bacterial and viral infections. Eugenol also reduces gut motility in diarrhea and has even been shown to inhibit platelet aggregation in vitro. In addition, acetyl eugenol, another component of clove oil, acts as a strong antispasmodic, which is helpful for easing coughs and, when applied topically, for relieving muscle spasms.1-6
Researchers from Minia University in Egypt tested various essential oils to determine their inhibitory effects on dermatophytic fungi—any of several fungi that cause parasitic skin disease in humans. Results showed that clove and peppermint oils provided strong fungistatic effects, seriously inhibiting the growth of tested fungi. Such impressive results led researchers to suggest adding clove and peppermint oils in antidermatophytic drugs. This study is another confirmation for what many aromatherapists already know—clove oil is an effective fungicide for athlete’s foot and scabies.3,7
The antimicrobial activity of clove bud essential oil has also been confirmed in several studies. For example, researchers examined several essential oils to determine their effect on enteropathogenic (microorganisms that cause disease primarily in the intestinal tract) and spoilage bacteria strains. The essential oils of clove bud (Eugenia caryophyllata) and thyme (Thymus vulgaris) proved to be particularly effective, providing a large spectra action. In addition, studies show clove bud oil also inhibits many oral bacteria such as Streptococcus sp.2,8,9
Researchers in France conducted a study to determine which essential oils would purify and deodorize the air, destroying bacteria such as Proteus, Staphylococcus aureus and Streptococcus pyogenes. Several vaporized essential oils were found to effectively destroy 90% of microbes within 3 hours, including clove, lavender, lemon, mint, pine, rosemary and thyme. Furthermore, in one randomized trial of 182 institutionalized patients, a mixture of the essential oils of clove, cinnamon, lavender, thyme and mint appeared to decrease the frequency of bouts of chronic bronchitis. One advantage of inhaling vaporized essential oils is that, in many cases, infections linger in the sinuses between bouts. Another study published in the Journal of Applied Bacteriology showed that the essential oil of clove had a definite germicidal effect against Candida albicans and various bacteria, including Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa, Clostridium perfringens, and Escherichia coli.1,2,10
Psychologically, clove oil provides an arousing, strengthening aroma, commonly used to combat frigidity and impotence, since it enhances libido by directly stimulating the reproductive genital organs. Clove oil is also equally energizing as a mental stimulant.3
Caution should be exercised when applying clove oil topically, as it can cause unpleasant or painful skin reactions in sensitive individuals. Clove oil is contraindicated for those with hypertension or abdominal pain and for those taking the maximum dosage of acetominophen, in order to avoid any possibility for potentiation of this medication. Individuals undergoing anticoagulant therapy should avoid using clove oil. Essential oils should be kept out of the reach of children, as a lethal dose of clove oil for a 3-year-old child is 19 ml. (taken orally).3
References: 1Buckle RGN, J. Clinical Aromatherapy in Nursing. San Diego, CA: Singular Publishing Group Inc., 1997. 2Schnaubelt PhD, K. Advanced Aromatherapy. Rochester, VT: Healing Arts Press, 1995. 3Damian, P. and Damian, K. Aromatherapy: Scent and Psyche. Rochester, VT: Healing Arts Press, 1995. 4Wagner, H., et. al. “In vitro inhibition of prostaglandin biosynthesis by essential oils and phenolic compounds.” Planta Medica; 1986, 3:184-187. 5Janssens, J., et. al. “Nutmeg oil: identification and quantitation of its most active constituents as inhibitors of platelet aggregation.” Journal of Ethnopharmacology; 1990, 29(2): 179-188. 6Chevallier, A. The Encyclopedia of Medicinal Plants. NY, NY: Dorling Kindersley, 1996. 7el-Naghy, M.A., et. al. “Fungistatic action of natural oils and fatty acids on dermatophytic and saprophytic fungi.” Zentralbl Mikrobiol; 1992, 147(3-4): 214-220. 8Ramanoelina, A.R., et. al. “Antibacterial action of essential oils extracted from Madagascar plants.” Arch Inst Pasteur Madagascar; 1987, 53(1): 217-226. 9Saeki, Y. “Antimicrobial action of natural substances on oral bacterial.” Bulletin of the Tokyo Dental College; 1989, 30(3): 129-135. 10Briozzo, J., et. al. “Antimicrobial activity of clove oil dispersed in a concentrated sugar solution.” Journal of Applied Bacteriology; 1989, 66(1): 69-75.
The assault continues. Air intensity continues at 9.25+ as I type this. The Barium type is still dominant. The power is still out from the huge windstorm yesterday.
10:45 am
We are now getting hit with a Burnt type plume.
~10:40 am Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.25, Rising
12:35 pm
A few minutes ago we were hit with a wide-spectrum plume:
~7 pm Event: Hit with wide-spectrum plume. This was dominated by the Barium and Mercury types. Components (strongest to weakest): - Barium - Dominant - Mercury - Second dominant - Inflammatory - Also very strong Intensity Delta: Medium-Fast Peak Intensity: 10
The last plume above was horrible and induced intense mercury symptoms. They layered this plume until about 8:45 pm when intensity finally began falling off.
It's now 10:10 pm and we are now having our nightly "break". Intensity is down to 7.25+ and it feels wonderful. After such a horrible day or spraying, this is a welcomed departure from the daily torture.
We were hit with a wide-spectrum plume at about 3 pm. They have been layering ever since keeping intensity at about 9.75. This is pretty brutal. Following is the event profile:
~3 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Chalky-Bitter-Pharma - This has been dominant. Usually the Model Cement type is dominant. - Model Cement/Burnt Plastic - See Microplastics - Inflammatory - Mercury Intensity Delta: Medium-Fast Peak Intensity: 10 Current Intensity (via layering); 9.75- as I type this.
5:52 pm
We were hit with a wide-spectrum plume at about 5 pm and a Burnt type plume at about 5:40 pm
We have been hit with a Burnt type plume a little bit ago.
~7:10 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 9
11:17 pm
Nearly every night around 10:30 pm we are hit with a plume. It's nearly always a gentle plume that slowly pushes intensity up. This is exactly what happened tonight.
Tonight at 10:27 pm we were hit with a wide-spectrum plume that is gently pusing intensity up. Following is the event profile:
~10:27 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Inflammatory - This type is dominant. - Chalky-Bitter-Pharma - This has been dominant. Usually the Model Cement type is dominant. - Model Cement/Burnt Plastic - See Microplastics - Mercury Intensity Delta: Medium-Slow Current Intensity: 8.5+, Rising
12:06 am (12/19)
Nearly every night around 11:30 pm we are hit with a plume. tonight it happened again. Following is the event profile:
~11:30 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Inflammatory - This type is dominant. - Chalky-Bitter-Pharma - This has been dominant. Usually the Model Cement type is dominant. - Model Cement/Burnt Plastic - See Microplastics - Mercury Intensity Delta: Medium-Slow Current Intensity: 9.25, Rising
12:19 am (12/19)
We are now getting hit with a Burnt type plume, as we do every night several times.
~12:10 am (12/19) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.25
Ambient intensity overnight was 7.5. We had no discrete plumes during the night that I am aware of.
We had the following plumes throughout the day:
~8:50 am - Hit with wide spectrum plume. Peak intensity: 9.5 ~11:30 am - Hit with wide spectrum plume. Peak intensity: 9.5
By about 1 pm intensity had been layered with the typical wide-spectrum components up to intensity 8 and remained at that intensity all afternoon.
Intensity finally returned to ambient by about 8 pm.
~8:30 pm - Hit with wide spectrum plume. Peak intensity 9.25.
From ~9:30 pm until 11:30 pm intensity fell to 6, the lowest it had been for a long time. All pain disappeared during this time. My eyesight improved dramatically. Mercury increases intraocular pressure changing the focal length of the eye inducing far/nearsightedness. Inflammation disappeared. A peaceful 2 hours without pain. This is the way I should be feeling all the time.
~11:30 pm - Hit with gentle wide spectrum plume that increased intensity slowly.
~1 am - Hit with wide-spectrum plume that differed from the typical mix. Following is the event profile:
~1 am Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Sharp Metallic - Mercury - Mercury is always very strong with the Sharp Metallic type. - Chalky-Bitter-Pharma - Inflammatory Intensity Delta: Medium-Fast Peak Intensity: 10
~2:53 am - Hit with wide spectrum plume. Peak intensity 10-.
We had wide-spectrum aerosols in the air throughout the night, as usual. Intensity was steady at 8-, just a little lower than the night before. Following is the list of aerosol types we were breathing while most slept:
We have been hit 3 times this morning. Once is occurring as I type this because it's now 11:35 am and they hit us at 11:30 am, as they do most mornings. These are all standard wide-spectrum plumes containing the following components:
~7:50 am Event: Hit with wide-spectrum plume. Intensity Delta: Medium-Fast Peak Intensity: 9.25+
~10 am Event: Hit with wide-spectrum plume. Intensity Delta: Medium-Fast Peak Intensity: 9.5+
~11:30 am Event: Hit with wide-spectrum plume. Intensity Delta: Medium-Fast Current Intensity: 9.5, Rising
So far, a pretty typical day with 3 pretty brutal plume producing nearly unbreathable air with many health symptoms associated with each one.
The day the world wakes up and realizes that most of their illnesses have been given to them by either one means or another, is the day change truly begins to take place, because realizing this is happening is 80% of the battle.
12:02 pm
We have been hit with our first Burnt type plume of the day:
~11:50 am (12/16) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.5+, Rising
1:05 pm
We have been hit with another wide-spectrum plume, right on schedule.
I have been logging all day but have not published the entries, so here they are now.
3:23 pm - Wide spectrum plume. 3:53 pm - Burnt Electronics/Fungal type plume, peaked over 8.75 5:30 pm - Wide spectrum plume. 5:35 pm - Burnt Electronics/Fungal type plume, peaked over 8.75 7:10 pm - Wide spectrum plume. Slow intensity delta. 9:50 pm - Wide spectrum plume. At 9:29 pm intensity reached 10. 10:27 pm - Burnt Electronics/Fungal type plume, 11:27 pm - Wide spectrum plume. Intensity is now (11:55 pm) 10.
12:19 am
12:14 am (12/17) - Hit with a wide-spectrum plume. Intensity is now 9.5 and rising. 12:15 am - Hit with a Burnt Electronics/Fungal type plume, Intensity is now 8.25+ and rising.
December 15 - The Daily Spraying Log Celebrities Who Work For Globs - Gastrointestinal Recovery - Chemtrails Will Help The Anti-Christ
The air last night was nearly identical the air the night before. We had wide-spectrum aerosols in the air throughout the night. Intensity was steady at 8, just a little lower than the night before. Following is the list of aerosol types we were breathing while most slept:
Studies show over 4 million people have ulcers. Many more suffer from chronic gastritis, with symptoms such as burning, cramping, and abdominal aching. These symptoms are often temporary, usually coming in waves and lasting for only 3-4 days at a time, with pain being worse prior to meals and at bedtime.
According to a study published in The New England Journal of Medicine, more than 90% of people having duodenal ulcers and 80% having gastric ulcers are infected with a bacteria known as Helicobacter pylori or H. pylori, for short. This bacteria has been found to suppress hydrochloric acid production, which would normally kill any bacteria and parasites in the stomach. When H. pylori invades stomach tissues, white blood cells respond to the area resulting in inflammation. Prolonged inflammation can destroy the stomach’s protective lining, as can H. pylori itself. This bacteria can break down the mucin—the stomach’s protective layer—allowing any available hydrochloric acid to come in contact with unprotected stomach tissues. In either case, the result is chronic superficial gastritis, with burning, pain and indigestion. Left untreated, this problem can escalate into a peptic ulcer, or worse, chronic atrophic gastritis, which can lead to stomach cancer. In fact, an article published in Contemporary Gastroenterology indicated 50% of patients with non-ulcer gastritis are diagnosed with an H. pylori infection.
Another study published in The New England Journal of Medicine, found over 90% of people suffering from stomach cancer have H. pylori specific antibodies in the bloodstream for an average of 13 years before diagnosis. Furthermore, those having H. pylori antibodies are 3 times more likely to develop stomach cancer during the next 1-24 years.
Capsicum supports the stomach during times of discomfort and distress. Capsicum stimulates blood circulation, induces perspiration, increases the production of digestive fluids, and relaxes muscle spasms. Capsicum is often used for colic, cold limbs, dropsy, flatulence, rheumatic arthritis, and ulcers.
Cloves extract (concentrated) stimulate circulation, increase the production of digestive and mucosal fluids, alleviate pain, and act as an antiseptic and local anesthetic, helping to relieve pain associated with infection and toothache. Cloves contain a volatile oil, comprised mostly of eugenol (a phenol), which has been shown to be strongly antibacterial. Numerous studies have demonstrated cloves’ antibacterial, anticandidal (Journal of Ethnopharmacology), antifungal, antimicrobial (Journal of Ethnopharmacology), and antiviral (Planta Medica) activities. Cloves are also commonly used to expel parasites and repel insects. Cloves’ antispasmodic properties, combined with their ability to enhance digestion, have been used to relieve abdominal distension (bloating), colic, cramping, and gas, as well as chronic coughs and muscle spasms. Recent research suggests possible benefit for treating peptic ulcers with cloves.
Deglycyrrhizinated licorice (DGL) extract provides nutrients essential for optimal digestive function. Studies have shown DGL is both safer and more effective in treating peptic ulcers than either Tagamet or Zantac, the two most popular prescription drugs. DGL is licorice root which has been stripped of a substance known as glycyrrhizin, which occurs naturally in the herb but has the ability to raise blood pressure and lower potassium levels in some individuals. DGL improves normal defense mechanisms in the stomach and intestinal cells, stimulates the production of cells which form the protective mucosal lining of the GI tract, encourages blood flow to this protective barrier, and increases the longevity of intestinal tract cells. In comparison, Tagamet and Zantac actually reduce stomach acid secretion and weaken these protective gastrointestinal functions.
A large study involving 874 individuals with chronic duodenal ulcers was conducted, with some receiving DGL, some Tagamet, and others given antacids. After six weeks, 77% of those on DGL were healed, compared to only 63% taking Tagamet. Furthermore, those receiving DGL had a reduced rate of relapse (recurrence of the ulcers), as their natural protective forces had been strengthened by DGL.
Inula racemosa (concentrated), a species of elecampane, has been found to be particularly effective against H. pylori bacteria. As with other varieties of elecampane, inula racemosa relieves indigestion and soothes the lining of the digestive tract with a starchy substance called inulin, which has been found helpful for treating ulcers. Inula racemosa also contains an essential oil which fights bacteria and fungi, and destroys and expels parasitic worms.
Pau d’arco powder extract (concentrated) is recommended by medical doctors in Brazil for its antifungal properties against ringworm, systemic Candida albicans yeast infections, and other gastrointestinal parasite infestations. Pau d’arco is rich in lapachol, an immuno-stimulant compound, which is responsible for much of the herb’s antibiotic properties.
At about 1 pm we were hit with a wide-spectrum plume that was dominated by the Stimulant type. This type makes you feel like you've been injected with adrenaline. It is a horrible feeling. Below is the event profile:
We have been hit with another wide-spectrum plume which is very strong right now. This plume also contains the Stimulant type but this time it is not the dominant type.
~3:11 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 9.25 Current Intensity: 8.5, Declining
6:07 pm
We have been hit again at about 5:50 pm. This is not the typical wide-spectrum plume that has the Model Cement/Burnt Plastic type dominating. Instead, his has the Barium type and the Sharp Metallic type dominating. The Sharp Metallic type causes a symptom set identical to mercury poisoning, including tinnitus (ringing in the ears). Following is the event profile:
~5:50 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Sharp Metallic - Causes strong mercury symptoms. - Barium - Usually sprayed in front of precipitation. - Inflammatory - Mercury Intensity Delta: Medium-Fast Peak Intensity: 9.75- Current Intensity: 9.5, Declining
7:21 pm
At about 6:55 pm we were hit with a more convention wide-spectrum plume which had the Model Cement/Burnt Plastic type as the dominant component. This it the typical wide-spectrum plume that we experience day-after-day. Below is the event profile:
After the 6:55 pm plume, intensity slowly dissipated. We had a long, but not so mild, break from about 9 pm until 11:30 pm. Intensity fell to 7.75- and remained there during that time.
We were hit at 11:30 pm, as we are most nights, with a typical wide-spectrum plume.
We were hit again at 12:14 am with a very powerful plume dominated by the Inflammatory and Mercury types. I have not experienced the Inflammatory type this powerful for months.
Following are the event profiles.
At about 6:55 pm we were hit with a more convention wide-spectrum plume which had the Model Cement/Burnt Plastic type as the dominant component. This it the typical wide-spectrum plume that we experience day-after-day. Below is the event profile:
~12:14 am (12/16) Event: Hit with wide-spectrum plume dominated by Inflammatory and Mercury types. Components (strongest to weakest): - Inflammatory - Strongest hit with this type we have had in months. This could really hurt people. - Mercury - Having very strong mercury symptoms as well. - Model Cement/Burnt Plastic - See Microplastics - Chalky-Bitter-Pharma Intensity Delta: Medium-Fast Peak Intensity: 10 (actual 11.5) Current Intensity: 9.5+, Declining
2:17 am (12/16)
We have been hit with 2 plumes since the previous entry. Following are the event profiles:
We had a wide-spectrum of aerosols in the air through the night, as usual. Intensity was steady throughout the night and was higher than usual at 8.25. Following is the list of aerosol types we were breathing while most slept:
If you have been following this log, you know that certain "specialty" aerosol types make an appearance for several days, then stop for several weeks. This cycle continues throughout the year. The Morgellon's aerosol type is one of those types, and it made its re-appearance this morning.
This type makes some people's skin itchy. It quite literally feels like you're getting bit by bugs, although not everyone experiences this symptom when exposed to this type.
We have had 2 events so far this morning. The first event included the Morgellon's type. Following are the event profiles:
As I'm typing this log entry, we are now (12:07 am) being hit with another plume (right on schedule), and this one again contains the Morgellon's type. Following is the event profile:
Both mercury and venom peptides block magnesium from being used by the body. Magnesium is necessary in order for your body to metabolize calcium. When you cannot metabolize calcium, you will likely get cavities.
On a side note, isn't it ironic how mercury has been used in dental fillings for decades, yet, mercury blocks magnesium and calcium metabolism. Ironically, these fillings, by off-gassing mercury, cause the very condition (cavities) they "treat".
This is an example of the highly-unethical machiavellian business model. This is the process of intentionally causing a problem and then profiting from the solution. This is the business model that has empowered the super-rich globalists to become super-rich. This, folks, is how they did it.
I know people who began getting cavities, for no known reason, before 2010. This is likely the same period of time they began spraying the Chalky-Bitter-Pharma type in some areas. Everything has a cause, and now we have a likely candidate.
Intentional Disasters
If you know nothing else about how the world really works, this is one fact that everyone must know to understand what is happening in the time we live in.
In order to scare the public into accepting changes that would normally be grossly unacceptable, globalists use fear. They generate fear by creating disasters. In the world, some things are complicated. Some things are simple. This is simple. This is how the world really works. This is how globalists gain public support—or actually the illusion of public support—to do things that are otherwise devastating for the public.
I will continue to expound upon this in future articles, but this short video provides and excellent 10,000-foot view of the plan the globalists have for the world, and exactly how they are implementing it now. Not in the future. Now, as you are reading this.
Magnesium is an essential mineral involved in nearly every function of the body. For example, magnesium is necessary for cardiac health, production of ATP (adenosine triphosphate, the molecule that provides energy for the cells), formation of bone and protein, healthy functioning of nerves and muscles, and the regulation of blood pressure and blood sugar levels—magnesium plays an important role in insulin secretion and function. Magnesium also helps maintain the acid-alkaline balance of the body and is necessary for calcium to function properly. Furthermore, magnesium is needed for healthy muscle, nerve and blood vessel tone and is thought to help prevent blood vessel spasms.1-5
Determining magnesium deficiency can often be difficult, as magnesium deficiency can present with many signs and symptoms. Symptoms of magnesium deficiency include anxiety, aggression, loss of appetite, convulsions/seizures, cramps, depression, fatigue, hearing loss, impotence, insomnia, muscle spasms, neuropsychiatric disturbances, nervousness, tremors and weakness. Animal studies have shown that magnesium deficiency also causes a significant increase in free radicals and subsequent tissue injury, decreases specific immune response, and accelerates the progressive degeneration of the thymus. In addition, magnesium deficiency can lead to cardiovascular disorders such as angina pectoris (chest pain caused by a lack of oxygen supply to the heart), cardiac arrhythmia (abnormal heart rhythm), hypertension (high blood pressure) and coronary artery disease (CAD)—a condition involving the progressive narrowing and hardening of the arteries, also known as atherosclerosis. In fact, cardiovascular diseases—cardiac arrhythmias, hypertension and heart failure—lead the list of disorders associated with hypomagnesemia (abnormally low blood levels of magnesium). Research shows that blood levels of magnesium are low in patients with coronary artery spasms (which deprive the heart muscle of blood flow and oxygen), myocardial ischemia (a heart condition caused by insufficient blood flow to the heart muscle), mitral valve prolapse (a type of heart disease in which the mitral valve fails to regulate blood flow between the left atrium and left ventricle of the heart), and cardiac tachyarrythmia (excessively rapid heartbeat accompanied by arrhythmia). Low tissue and blood levels of magnesium have also been documented in patients prior to, during and after myocardial infarction (heart attack). Plus, recent studies have implicated the lack of sufficient magnesium as a cause of hypertension and preeclampsia—a condition of hypertension occurring in pregnancy, accompanied by edema (fluid retention) and proteinuria (protein in the urine)—in pregnant women. A 2003 study involving 63 middle- to upper-income pregnant women confirmed that participants’ intake of magnesium was suboptimal.1-4,6-13
Magnesium deficiency is common among individuals taking antibiotics, oral contraceptives, "potassium-depleting“ prescription drugs (i.e. loop and thiazide-like diuretics), or too many laxatives. However, dietary magnesium intake among the general population is also often suboptimal—estimates indicate that as much as 60% of the U.S. population may be at risk for magnesium deficiency.2,7,13
Fortunately, magnesium supplementation has been used successfully to treat a wide range of medical problems, including asthma, chronic fatigue syndrome, migraines, heart disease and cardiac arrhythmias, and certain types of urinary incontinence. Magnesium therapy is rapid-acting, has a safe toxic-therapeutic ratio, and is easy to administer and monitor. Plus, clinical use of magnesium in preeclampsia and acute myocardial infarction confirms its safety and tolerability.6,14,15
Research has shown that magnesium levels are chronically low in asthmatics. Magnesium is necessary to help relax the bronchial tubes and smooth muscle of the esophagus, and evidence supports its use in severe asthma. A study of magnesium concentrations in 25 patients with bronchial asthma, compared to 9 age-matched healthy subjects, revealed magnesium deficiency in total body stores in 40% of asthmatic patients and only 11% of healthy participants. Findings from another study demonstrated a strong positive correlation between intracellular magnesium and the level of bronchial reactivity—intracellular magnesium concentrations in the group of patients with mild-to-moderate asthma were significantly lower than the non-asthmatic subjects.16-20
Magnesium also appears to play a significant role in the pathogenesis (origin and development) of migraines. According to research, as many as 50% of migraine sufferers are magnesium-deficient. In a 1996 German study of 81 migraine patients, 41.6% of participants taking oral magnesium experienced a reduction of both the duration and intensity of migraine attacks, as well as reduced their reliance on medications to control their migraines. In 2003, results from a randomized, double-blind, placebo-controlled, parallel-group trial involving 86 children (ages 3-17) were published. The participating children all reported a 4-week history of at least weekly, moderate-to-severe headaches with a throbbing or pulsatile (beating) quality, associated anorexia/nausea, vomiting, photophobia (aversion to light), sonophobia (aversion to sound), or relief with sleep, but no fever or evidence of infection. Oral magnesium supplementation (9 mg/kg divided among 3 meals daily for 16 weeks) resulted in a statistically significant decrease over time in the frequency of headaches, with no decrease observed in the placebo group, as well as significantly lower headache severity relative to the placebo group. Two other double-blind studies also indicate that chronic oral magnesium supplementation may reduce the frequency of migraine headaches.5,21-24
In addition, magnesium demonstrates a protective effect against stress-induced physiologic damage. Research has shown a negative correlation between magnesium balance and oxidative stress—chronic stress or injury lowers magnesium levels while simultaneously increasing the intensity of oxidative stress upon the body. Both magnesium deficiency and oxidative stress have been identified as pathogenic factors in aging and in several age-related diseases, such as stress-induced cardiovascular damage. When magnesium deficiency exists, stress paradoxically increases the risk of cardiovascular damage, including arrhythmias, hypertension, cerebrovascular and coronary constriction and occlusion (tightening and closure/obstruction of the blood vessels of the brain and arteries that supply the heart), and sudden cardiac death (death resulting from an unexpected and abrupt loss of heart function). Thus, stress, whether physical (i.e. cold, heat, burns, accidental/surgical trauma, or physical exertion) or emotional (i.e. anxiety, pain, excitement or depression), as well as stress resulting from dyspnea (difficulty of breathing) as in asthma, increases the need for magnesium. However, magnesium therapy has been shown to significantly increase intracellular magnesium levels, compared with placebo, to reduce stress-induced oxidative damage. For example, a 6-month randomized, double-blind, placebo-controlled trial of 187 patients with coronary artery disease (CAD) found that magnesium supplementation (365mg of magnesium citrate per day) significantly increased exercise duration time (exercise tolerance) compared to placebo, and lessened exercise-induced chest pain. Quality-of-life parameters also significantly improved in the magnesium group.25-31
Magnesium deficiency is also common among patients with renal (kidney) stones. Research has shown a clear inverse correlation between magnesium concentration and the formation of calcium oxalate crystals, which grow in the urinary tract to form more than 70% of kidney stones. A multicenter clinical investigation involving postmenopausal women identified 1,179 cases of kidney stones, with one of the three primary risk factors for the occurrence of kidney stones being a low dietary intake of magnesium. Studies have shown that magnesium acts as an inhibitor of calcium oxalate crystallization—magnesium helps increase the solubility of calcium oxalate crystals and increases urinary calcium excretion by inhibiting renal calcium reabsorption. Thus, magnesium supplementation is suggested in order to prevent deficiency and the recurrence of stone formation.32-42
The best forms of supplemental magnesium appear to be those chelated to an amino acid or a Krebs cycle intermediate such as citrate or malate. Krebs cycle intermediates are compounds utilized in the Krebs cycle (also known as the citric acid cycle), the metabolic process that produces energy within the cells. These forms of supplemental magnesium appear to be better utilized, absorbed and assimilated than inorganic mineral forms (i.e. carbonates, chlorides, oxides).In fact, research has shown that magnesium citrate is more soluble and more bioavailable, with respects to gastrointestinal absorbability, than magnesium oxide.38,43-46
References: 1Lininger DC, S., et al. The Natural Pharmacy, 2nd ed. Rocklin, CA: Prima Health, 1999. 2Lieberman, S. & Bruning, N. The Real Vitamin & Mineral Book. Garden City Park, NY: Avery, 1990. 3Dunne, L.J. Nutrition Almanac, 3rd Ed. NY, NY: McGraw-Hill Publishing Co., 1990. 4Pizzorno, J. & Murray, M. Textbook of Natural Medicine, 2nd ed. London: Churchill Livingstone, 1999. 5Schuck, P., et. al. [Migraine and prevention of migraine: the value of magnesium]. Schweizerische medizinische Wochenschrift; 1999, 129(3):63-70. 6Gailing CN, S. "If You Had To Recommend Just One Supplement Product To Customers Or Colleagues, What Would It Be And Why?“ Nutrition Science News; September 2000. 7Bohl, C.H. & Volpe, S.L. "Magnesium and exercise.“ Critical Reviews in Food Science and Nutrition; 2002, 42(6):533-563. 8Bergner, P. The Healing Power of Minerals, Special Nutrients, and Trace Elements. Rocklin, CA: Prima, 1997. 9Johnson, S. "The multifaceted and widespread pathology of magnesium deficiency.“ Medical hypotheses; 2001, 56(2):163-170. 10Petrault, I., et. al. "Changes in gene expression in rat thymocytes identified by cDNA array support the occurrence of oxidative stress in early magnesium deficiency.“ Biochimica et Biophysica Acta; 2002, 1586(1):92-98. 11Malpuech-Brugere, C., et. al. "Accelerated thymus involution in magnesium-deficient rats is related to enhanced apoptosis and sensitivity to oxidative stress.“ The British Journal of Nutrition; 1999, 81(5):405-411. 12Bernstein MD, L. "Improving Magnesium Absorption and Bioavailability.“ Geriatric Times; 2002, 3(1). 13Turner, R.E., et. al. "Comparing nutrient intake from food to the estimated average requirements shows middle- to upper-income pregnant women lack iron and possibly magnesium.“ Journal of the American Dietetic Association; 2003, 103(4):461-466. 14Crippa, G., et. al. "Magnesium and cardiovascular drugs: interactions and therapeutic role.“ Annali Italiani di Medicina Interna; 1999, 14(1):40-45. 15Muir KW. "Magnesium for neuroprotection in ischaemic stroke: rationale for use and evidence of effectiveness.“ CNS Drugs; 2001, 15(12):921-930. 16Broadhurst PhD, C.L. "Natural Asthma Relief.“ Nutrition Science News; April 1999. 17Durlach, J. "Magnesium depletion, magnesium deficiency, and asthma.“ Magnesium Research; 1995, 8:403-405. 18Kaye, P. & O'Sullivan, I. "The role of magnesium in the emergency department.“ Emergency Medicine Journal; 2002, 19(4):288-291. 19Hashimoto, Y., et. al. "Assessment of magnesium status in patients with bronchial asthma.“ The Journal of Asthma; 2000, 37(6):489-496. 20Dominguez, L.J., et. al. "Bronchial reactivity and intracellular magnesium: a possible mechanism for the bronchodilating effects of magnesium in asthma.“ Clinical Science (London); 1998, 95(2):137-142. 21Mauskop, A. & Altura, B.M. "Role of magnesium in the pathogenesis and treatment of migraines.“ Clinical Neuroscience; 1998, 5(1):24-27. 22Peikert, A., et al. "Prophylaxis of migraine with oral magnesium: results from a prospective multicenter, placebo-controlled and double-blind randomized study.“ Cephalalgia; 1996, 16:257-263. 23Friedrich PhD, J. "Stop The Pain: Natural Remedies For Migraines.“ Nutrition Science News; June 1999. 24Wang F, et. al. "Oral magnesium oxide prophylaxis of frequent migrainous headache in children: a randomized, double-blind, placebo-controlled trial.“ Headache: The Journal of Head and Face Pain; 2003, 43(6):601-610. 25Ronzio PhD, R.A. "Nutritional support for adrenal function.“ American Journal of Natural Medicine; 1998, 5(5):12-17. 26Galland, L. "Magnesium, stress and neuropsychiatric disorders.“ Magnesium and Trace Elements; 1991-92, 10(2-4):287-301. 27Cernak, I., et. al. "Alterations in magnesium and oxidative status during chronic emotional stress.“ Magnesium Research; 2000, 13(1):29-36. 28—. "Characterization of plasma magnesium concentration and oxidative stress following graded traumatic brain injury in humans.“ Journal of Neurotrauma; 2000, 17(1):53-68. 29Manuel y Keenoy, B., et. al. "Magnesium status and parameters of the oxidant-antioxidant balance in patients with chronic fatigue: effects of supplementation with magnesium.“ Journal of the American College of Nutrition; 2000, 19(3):374-382. 30Seelig, M.S. "Consequences of magnesium deficiency on the enhancement of stress reactions; preventive and therapeutic implications (a review).“ Journal of the American College of Nutrition; 1994, 13(5):429-446. 31Shechter, M,, et. al. "Effects of oral magnesium therapy on exercise tolerance, exercise-induced chest pain, and quality of life in patients with coronary artery disease.“ American Journal of Cardiology; 2003, 91(5):517-521. 32Reungjui, S., et. al. "Magnesium status of patients with renal stones and its effect on urinary citrate excretion.“ BJU International; 2002, 90(7):635-639. 33Hallson, P.C., et. al. "Magnesium reduces calcium oxalate crystal formation in human whole urine.“ Clinical Science (London); 1982, 62(1):17-19. 34Ferrari, L., et. al. [Etiopathogenesis and clinical aspects of nephrolithiasis--at present]. Recenti Progressi in Medicina; 2003, 94(3):136-141. 35Hall, W.D., et. al. "Risk factors for kidney stones in older women in the southern United States.“ American Journal of the Medical Sciences; 2001, 322(1):12-18. 36Worcester, E.M. "Stones from bowel disease.“ Endocrinology and Metabolism Clinics of North America; 2002, 31(4):979-999. 37Grases, F., et. al. "Dietary effects upon calcium oxalate urolithiasis risk.“ International Urology and Nephrology; 1992, 24(5):495-501. 38Lukaczer ND, D. "Nutrition Q & A with Dan Lukaczer, N.D.“ Nutrition Science News; December 1999. 39Heller, H.J. "The role of calcium in the prevention of kidney stones.“ Journal of the American College of Nutrition; 1999, 18(5 Suppl):373S-378S. 40Revusova, V., et. al. "Impaired renal tubular reabsorption of magnesium (TRMg) in Ca-containing kidney stone formers.“ International Urology and Nephrology; 1984, 16(3):237-242. 41Kato, Y., et. al. [A case of urolithiasis associated with short bowel syndrome]. Nippon Hinyokika Gakkai zasshi(The Japanese Journal of Urology); 2003, 94(1):33-36. 42Viterbo, R. & Mydlo, J.H. "Incidence and management of dialysis patients with renal calculi.“ Urologia Internationalis; 2002, 69(4):306-308. 43Rehan, J. "Magnesium: The Multi-Purpose Mineral.“ Think Muscle; 2001. . Accessed November 2003. 44Openlander, D. "Herbal Remedies For Reproductive Concerns.“ Natural Foods Merchandiser; February 2002. 45Murray ND, M.T. Encyclopedia of Nutritional Supplements. Rocklin, CA: Prima Publishing, 1996. 46Lindberg, J.S., et. al. "Magnesium bioavailability from magnesium citrate and magnesium oxide.“ Journal of the American College of Nutrition; 1990, 9(1):48-55.
Daily Spraying Log Continued
2:51 pm
We have been hit with another wide-spectrum plume:
Soon after the previous plume hit us, 2 components rose in intensity. They became dominant and remained dominant for about 90 minutes and then began to dissipate slowly. Following is the type profile for those 2 plumes:
Both of these are among the worst types for the symptoms they cause.
The TYPE II Biologics type make you body hurt as if you have the fully blown flu but without the fever and without any respiratory issues.
The Copper type causes headaches, nausea, vertigo, stomach issues, and much more.
From about 9:30 pm until now, we have had our nightly "break". Tonight, intensity dropped to 7.5. This is not low enough to relieve all the pain, but it does provide some relief.
As I type this (11:41 pm), intensity is increasing as we have been hit with another wide-spectrum plume. We normally get hit at about 11:30 pm most nights, so this is pretty much right on time.
We were hit with 2 plumes at nearly the same time: A wide-spectrum plume and a Burnt type plume. They hit us every night at about 1:30 am, so this was expected.
We had a stronger-than-usual night of spraying. Both the intensity and component mix was different than it has been
Throughout the night intensity was a very steady—and pretty strong—8.25. Intensity did not change until just after 9 am when it began falling slowly.
The component mixture was different as well. Usually the Model Cement/Burnt Plastic type dominates all night. Last night the Inflammatory and Mercury types dominated throughout the night. Following is the complete type profile overnight:
By 9:30 am, intensity had dropped to a tolerable—albeit still toxic—7.75. Then at about 11:20 am we were hit with the usual morning plume. Then we were hit again at about 12:30. Both of these events happened at the typical times they hit us most mornings. Below are the event profiles.
Lysine is an essential amino acid necessary for proper growth, enzyme production, protein synthesis, tissue repair, collagen formation, and the production of the amino acid, carnitine. Lysine assists calcium absorption, and helps maintain healthy functioning of the mammary and pineal glands and ovaries. Typical symptoms of lysine deficiency include cold sores, fever blisters, and stomach ulcers.
Lysine has been shown to inhibit the growth and replication of the herpes simplex virus (types I and II). This virus results in persistent outbreaks of a cyclical nature, recurring more frequently due to increased levels of stress or prolonged exposure to the sun. Following initial transmission and outbreak of sores, the herpes virus accumulates in nearby nerves and spinal ganglia, which offer protection against circulating antibodies. In essence, the herpes simplex virus is considered by some researchers as ganglionitis, as each recurrent case of herpes outbreak begins in the ganglion cells, traveling down the nerves to cause an eruption on the skin or mucus membrane.
Herpes simplex type I can cause cold sores and fever blisters to break out on the lips, inside the mouth and nostrils, and even on the eyelids and fingers, while type II results in genital sores. The herpes simplex virus has also been connected with the cause and proliferation of cancer, including lymphoma. Herpes simplex type II has been identified as one of the causes of cervical cancer.
Lysine has also been found to inhibit the virus responsible for outbreaks of shingles (herpes zoster) and assists in the treatment of measles, which is related to the herpes virus. Lysine supplementation, along with vitamin C, may aid treatment of certain viruses, including adenovirus I and II, cytomegalovirus (CMV), rubella (German measles), varicella (chickenpox), and variola (smallpox). Research shows sustained, relatively high doses of lysine have been effective in increasing the length of time between herpes outbreaks or entirely eliminating such outbreaks.
Lysine occurs naturally in beans, beef, brewer’s yeast, cheese, chicken, eggs, fish, milk, pork, potatoes, and tofu, and in the herbs, comfrey and fenugreek. Lysine is easily damaged by heat and is therefore, not present in processed foods.
Most nutritionists recommend 500-1,000mg of lysine daily to prevent or reduce herpes simplex outbreaks, and 1,000mg three times daily at the initial signs of acute recurrence. This same dosage has also been used for chronic Epstein-Barr virus infections (a virus belonging to the herpes family). To inhibit cases of shingles, 2,000-3,000mg of lysine daily is most often recommended.
~4 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75, Rising
5:24 pm
We have now been hit with another wide-spectrum plume. The previous wide-spectrum plume was at 3:15 pm. This one hit us at about 5:10 pm, so this has occurred on about a 2-hour interval. The component mix has changed, however. The Stimulant and Chalky types are now dominant (see below).
We have also just been hit with another Burnt type plume. The previous Burnt type plume hit us at 4 pm, so this has occurred on about a 1-hour interval. This interval is typical for this plume type in the evening.
~5:10 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9, Rising
6:44 pm
I have said frequently that I believe there are at least 2 separate spraying programs enacted for different purposes. One is most certainly for depopulation (why else would you spray known poisons on the population?). The other is for weather control (Barium salts are used in weather control and dissipation).
We have just been hit with ha plume that is not on a 2-hour interval that contains the Barium type. Because they have been using the 2-hour interval for the entire afternoon, you may expect that it would continue, but because the Barium-containing plume is not part of the same program, you must look at the pattern for the 2 programs independently. When you do this, the patterns emerge.
Having said this, we may expect another wide-spectrum plume, which will not contain the Barium type, at about 7:15 pm. This plume is part of the depopulation program so there is no temporal relationship between plume of different programs. I hope that makes sense.
Following is the event profile for the Barium-containing plume we just got hit with. Barium plumes almost always precede precipitation, so I'm going to check radar and see what is headed our way.
I just checked and what I saw was the remnants of a large system that has already been largely hypernucleated (sprayed to dissipation) before reaching us. It's sort of ironic because the predictive computer model shows a large, dense system, but actual radar show a spotty, 70% dissipated system.
Why the discrepancy because actual radar and predictive radar?
Because the predictive model does not have knowledge of the spraying, so it is showing what would have happened if no spraying existed. It's amazing that all these artifacts are right in front of our faces.
~6:40 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Barium - Inflammatory - Mercury Intensity Delta: Medium-Fast Current Intensity: 9+, Rising
7:49 pm
We have been hit with another wide-spectrum plume. We expected this at around 7:15 pm, but it's about 25 minutes later.
~7:45 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75, Rising
8:50 pm
So now we are getting hit on a 1-hour interval. This is another wide-spectrum, but it is a different mix than usual. This is identical in composition to the one we had at 5:10 pm this afternoon. Perhaps I should begin giving each "mix" it's own name.
In this one, the Stimulant and Chalky types are dominant. Not good.
You can almost set a watch by some of these plumes.
From about 9:30 pm until 11:23 pm we had an amazing "break". Intensity dropped to 7. All my inflammation went away, pain went away, and peace filled my body. It is a completely different kind of existence. This is how I would feel all the time if we weren't getting sprayed day-after-day.
They have ruined my life. They have destroyed many lives. One day the world will know the depths of wickedness in those who run the world.
So, at 11:23 pm we were hit with a wide-spectrum plume. It was not super powerful, but it was potent enough to ruin my night... again.
After the last plume of last night, intensity dropped to 7.5-, which is a little milder than usual, and remained there until about 7:30 am.
We have been hit with wide-spectrum plumes this morning at about the following times:7:30 am, 9:30 am, 11:30 am. Intensity peaked between 8.75 and 9 for each plume.
Intensity as I type this is 8.25+. It's about 1 pm so I'm expecting to get hit soon, and then they will likely layer all afternoon keeping intensity up.
Protease Enzymes have been shown to improve protein digestion, reduce inflammation, speed the healing of wounds, inhibit the formation of blood clots, and improve immune function. Protease Plus also provides beet root fiber and a trace mineral concentrate, since many vitamins, trace elements and minerals function as enzyme activators.
Enzymes are essential nutrients that initiate virtually all of the chemical reactions occurring within the body. Enzymes also aid in the elimination of toxins, including potentially harmful allergens and environmental pollutants. Unless obtained in the diet (from raw fruits and vegetables or dietary supplements), the constant demands on the body to manufacture enzymes can cause enzyme deficiency—a common problem that can lead to digestive dysfunction, cardiovascular disease, obesity, cancer and other illnesses. For example, enzyme deficiency is believed to be part of the mechanism that enables cholesterol deposits to accumulate along the inside of arterial walls, ultimately manifesting in heart disease.1-4
Incomplete digestion can be a major contributor to the development of numerous disease conditions. Approximately 58% of the population is believed to suffer from some type of digestive disorder. Not only can digestive dysfunction lead to nutritional deficiency and upset of healthy bowel flora, but in addition, incompletely digested macromolecules can be absorbed into the systemic circulation (the bloodstream). This can lead to a variety of immune complex diseases and is theorized to play an integral role in the etiology (origin) of food allergies. Antigenic (capable of producing an immune response) macromolecules can trigger the body’s defenses against exposure to what is perceived as foreign protein, thus producing symptoms of allergy. Furthermore, incompletely digested protein creates a favorable environment for “unfriendly” colonic bacteria, many of which create toxic substances that are absorbed by the body.4-6
Protease enzymes—also referred to as proteolytic enzymes—break down proteins into single amino acids. Proteases are capable of breaking down 300 grams of protein per hour. However, protease supplementation is beneficial for more than just improving digestion. Numerous human studies show that supplemental proteases given orally are absorbed intact into the bloodstream where they are able to act systemically—a process known as resorption. In this way, protease enzymes are used to treat acute inflammatory conditions such as sports injuries, surgery and wounds; reduce and eliminate food allergies; fight cancer and infections, including viral infections such as shingles (Herpes zoster) and AIDS; and combat auto-immune diseases such as rheumatoid arthritis, multiple sclerosis and scleroderma. Research also shows that protease is largely responsible for keeping the small intestine free of parasites, including bacteria, intestinal worms, protozoa and yeast. Thus, a lack of protease can greatly increase the chances of intestinal infection, including the overgrowth of the yeast Candida albicans.1,7-10
Protease is also an important component in preventing both tissue damage during inflammation, as well as the production of fibrin clots. Protease increases the breakdown of fibrin—a process known as fibrinolysis. Fibrin promotes inflammation by forming a wall around the area of inflammation, blocking blood and lymph vessels and causing swelling. Increased fibrin formation is also believed to be associated with production of cholesterol and fatty material, which inhibit circulation and contribute to heart disease. In addition, fibrin can cause blood clots to develop, which, if they become dislodged, can cause strokes or heart attack. Therefore, protease enzymes are often used therapeutically to treat thrombophlebitis—a disease where blood clots develop in veins, the veins become inflamed, and the clots dislodge, causing a stroke or heart attack.1,5,8,9
Protease’s ability to dissolve fibrin is also beneficial in the treatment of cancer. Cancer cells are covered with a thick “coat” of adhesive fibrin (referred to as “fibrin masking”), thus making the cancerous cells no longer recognizable by the body’s immune cells. In response, protease effectively dissolves the fibrin coating of the cancer cells, exposing their antigens to destruction by macrophages and the entire immune system. European oncologists have, for many years, included enzyme supplements as a natural, non-toxic adjuvant therapy against cancer; while nearly all of the leading alternative cancer specialists treating Americans prescribe enzymes as either primary or adjuvant cancer therapies. Furthermore, the National Cancer Institute is reportedly funding a large-scale study on the value of oral enzyme supplementation for cancer treatment.1,4,5,10,11
A 2-year pilot study of 11 patients with inoperable pancreatic adenocarcinoma (pancreatic cancer) led to significantly increased survival using large doses of proteolytic enzymes, combined with an aggressive nutritional therapy. The National Cancer Data Base reports that survival rates for all stages of pancreatic cancer are 25% survival at 1 year and only 10% survival at 2 years. However, 9 patients (81%) in the pilot study survived 1 year and 5 patients (45%) survived 2 years. Additionally, 4 patients were still living at 3 years.1,12
Furthermore, protease enzymes are essential for preventing the deposit of immune complexes in body tissues. Immune complexes are inflammatory byproducts of antibody attacks on antigens that are normally eliminated from the bloodstream by macrophages. Immune complexes that continue to circulate can be deposited in tissues where they can cause significant local tissue damage. Diseases such as AIDS, ankylosing spondylitis (arthritis of the spine), Crohn’s disease, lupus erythematosus, multiple sclerosis, pulmonary fibrosis, rheumatoid arthritis, scleroderma, and ulcerative colitis are associated with high levels of circulating immune complexes. Fortunately, both experimental and clinical studies show that protease preparations are extremely effective in decreasing levels of circulating immune complexes and activating macrophages to break up and eliminate them. Clinical improvements have been shown to correspond with reductions in immune complex levels.1,5,9,13
References: 1Cichoke DC, A. Enzymes & Enzyme Therapy, 2nd Ed. Los Angeles, CA: Keats, 2000. 2Balch MD, J. & Balch, P. Prescription for Nutritional Healing. Garden City Park, NY: Avery, 1990. 3Dunne, L. Nutrition Almanac, 3rd edition. NY, NY: McGraw-Hill, 1990. 4Bitomsky, M. “Digestive Enzymes: The Missing Link.” Life Extension Magazine; 1999, 5(4). 5Pizzorno J, Murray, M & Barrie, S (eds). A Textbook of Natural Medicine. Seattle, WA: Bastyr University, 1994. 6Lininger DC, S., et al. The Natural Pharmacy. Rocklin, CA: Prima Health, 1998. 7Cichoke DC, A. The Complete Book of Enzyme Therapy. Garden City Park, NY: Avery, 1999. 8Wright MD, J. Dr. Wright’s Guide to Healing with Nutrition. Emmaus, PA: Rodale Press, 1984. 9Murray ND, M. Encyclopedia of Nutritional Supplements. Rocklin, CA: Prima Publishing, 1996. 10“Leading European Oncologist Discusses Systemic Oral Enzyme Therapy & Cancer.” The Doctor’s Prescription For Healthy Living; 2000, 4(4). 11“How Systemic Oral Enzymes Inhibit Cancer Spread.” The Doctor’s Prescription For Healthy Living; 2000, 4(5). 12Gonzalez NJ & Isaacs, LL “Evaluation of pancreatic proteolytic enzyme treatment of adenocarcinoma of the pancreas, with nutrition and detoxification support.” Nutrition and Cancer; 1999, 33(2): 117-124. 13Cichoke DC, A. “Enzyme Therapy for MS Patients.” Nutrition Science News, May 1999.
The Daily Spraying Log - Continued
1:50 pm
We are getting hit with a Burnt type plume:
~1:45 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.5+, Rising
5:54 pm
We have just been hit with a wide-spectrum plume. They have been layering the intensity of the air so intensity has been at 8.25+ for a while, but this discrete plume is raising intensity quickly now.
The intensity of the previous wide-spectrum plume is now 9.75 and still rising.
8:18 pm
The intensity of the previous wide-spectrum plume is now 10.
11:39 pm
The previous plume finally dissipated by about 9:15 pm. Air intensity dropped to 7.25+ for a couple hours, and it was wonderful. All my aches and pains and fatigue that I live with disappeared.
Why did they disappear?
Because they are all caused by the spraying... All of it.
People have no idea how much of a role the spraying has in illness and disease, because of the simple fact that they cannot smell or taste it in the air. And this is why I do what I do. I smell and taste it and so it's my responsibility to expose this historic crime against humanity.
So, our little 2-hour break was wonderful, but at about 10:20 we were hit with a slow-rising, wide-spectrum plume that is now up to intensity 9- and still rising. And this is where we stand right now. Pretty strong poison in the air. It's hard to breath. It burns my sinuses. It makes everything hurt and much more.
It was a stronger than usual night of spraying. Although we had no discrete plumes, intensity was between 7.75 and 8.25 all night with all the usual toxic components they release into the atmosphere day-after-day.
We have already been hit with several plumes this morning and afternoon, plus they are now layering to keep intensity high without breaks They are using the typical wide-spectrum mix of components they normally use.
Following are the event profiles for the day so far:
They are layering so the intensity since the previous plume has remained between 9 and 9.5. As I type this, intensity is 9.5- with the Model Cement/Burnt Plastic type being the most potent component.
3:35 pm
~3:25 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.5+, Rising
4:09 pm
~4 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.5+, Rising
5:34 pm
I failed to mention this earlier, but they have been layering in TYPE III Biologics for the past few hours. This is the type that makes your body feel like you have the flu (aches, pains, fatigue), but there is no fever or runny nose, etc. Very bizarre.
5:46 pm
Even though they have been layering to keep intensity high, we are still getting hit with plumes that push intensity higher.
~6 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9-, Rising
7:30 pm
We have been hit with another Burnt type plume:
~7:20 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.25, Rising
11:04 pm
At about 8:46 pm we were hit with a wide-spectrum plume that peaked at intensity 9.5.
Between about 9:45 pm and 10:35 pm we had our nightly break. Intensity fell to 7.5. As usual, the health symptoms we suffer from the intentional poisoning of the air subsided somewhat, and it was a nice, albeit small, break.
At about 11 pm we were hit with another wide spectrum plume. Intensity is now 9 and rising.
Those who have decided to know nothing about what evil their passivity has bred will experience a sadly-rude awakening when they are eventually forced to discover how the world really works. I would have preferred we all learned the easy way. Unfortunately, many will learn the hard way.
11:24 pm
We are now getting hit with a Burnt type plume. Following is the event profile:
~11:20 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75, Rising
12:59 am (12/12)
We are now getting hit with yet another Burnt type plume. Following is the event profile:
~11:53 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9, Rising
It was a stronger than usual night of spraying. This was no surprise because of this pattern:
When we have a 12-hour section of milder-than-usual air, it is normally followed with stronger air, and that is precisely what happened last night.
Intensity was between 8 and 8.5 throughout the night. The air contained the typical wide-spectrum mix, except that it also contained TYPE I (cold-symptom inducing) Biologics.
We have been hit with 1 wide-spectrum plume this morning at a very common hit time: ~10:30 am. Following is the event profile:
Folate (vitamin B9) is an essential nutrient for numerous bodily functions, including normal development of the nervous system, cell replication, homocysteine and amino acid metabolism, glutathione production, and DNA synthesis, repair and methylation processes, which are crucial for maintaining healthy cellular and cognitive functions—impaired DNA methylation has been associated with a variety of psychiatric and neurological disorders such as schizophrenia, bipolar disorder, and other mental impairments. Sufficient folate is particularly critical prior to and throughout pregnancy for the health of both the mother and the developing child. Since humans cannot synthesize folate, it must be obtained through supplementation or from dietary sources. Folate occurs naturally in some foods such as green leafy vegetables, dried beans, peas, dietary fibers, egg yolks and liver. Unfortunately, maintaining optimal folate levels through diet alone is difficult, since up to 70% of folate is lost during cooking.1,2,5,8,9,13-26
Folate deficiency is surprisingly common, with studies suggesting deficiency rates as high as 85%, especially in women of child-bearing age. Lower serum folate levels have also been found in the elderly, in individuals who smoke or have higher alcohol intakes, and in patients with obesity and diabetes. Folate deficiency is associated with an increased risk of birth defects (neural tube defects) and other pregnancy complications (e.g. miscarriages, premature births, low birth weights, preeclampsia), as well as cardiovascular disease, cognitive dysfunction, neuropsychiatric disorders such as depression and dementia, and some cancers. A growing body of research also suggests that maternal folate deficiency may increase risk of autism spectrum disorders. Folate deficiency can result from low dietary intake (gluten-free diets are a poor source of folate), poor absorption of ingested folate, or altered folate metabolism due to drug interactions (e.g. oral contraceptives, metformin, anticonvulsant drugs) or genetic defects. Although estimates vary, research suggests that roughly half of the general population, particularly those of northern European, Hispanic, Mediterranean and northern Chinese descent, may carry a genetic mutation (e.g. MTHFR gene defect) that greatly reduces the body’s ability to absorb and utilize folate.1-5,8,9,13,15-19,22,25-37
Since folate is a vital component for human health, numerous countries have implemented food fortification measures (e.g. enriched flour, breads, cereals and pasta) to increase folate intake. However, fortified foods and most vitamin supplements utilize a synthetic form of folate known as folic acid, which is not naturally found in the human body. When folate is ingested, either as a natural food source or as synthetic folic acid, it must be enzymatically converted into its bioactive form as l-5-methyltetrahydrofolate, also known as l-methylfolate or 5-MTHF. Increasing evidence has shown that supplementation with l-methylfolate has many important advantages over synthetic folic acid. L-methylfolate is well-absorbed from the gastrointestinal tract; it has a higher bioavailability compared to synthetic folic acid; it’s bioavailability is not affected by metabolic or genetic defects; and it’s bioavailability is not hampered by drug interactions that inhibit synthetic folic acid metabolism. In addition, l-methylfolate is the only form of folate able to cross the blood-brain barrier where it plays an important role in the production of brain neurotransmitters (e.g. dopamine, norepinephrine, serotonin) that regulate mood and behavior.1,2,5,8,9,13,16-18,24,26,40-44
The Daily Spraying Log - Continued
12 noon
We are usually hit at noon each day, and this day is no exception. Below is the event profile for what is happening right now:
The intensity of the previous plume is now 9.5+ and still rising.
11:28 pm
We have been hit with a plume of type Burnt Electronics/Fungal:
~11:20 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.25, Rising
I didn't have time to write many comments earlier, but this has been another unique day. Notice that we did not have discrete plumes most of the afternoon. This happened yesterday, but is otherwise very rare. Are their assets occupied with the incoming storm?
12:37 am (12/11)
We have been hit with a plume of type Burnt Electronics/Fungal:
~12:30 am (12/11) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.25+, Rising
I'll get straight to the point. At roughly 4 am last night we were hit with TYPE III Biologics and they continued using this type throughout most of the morning.
No surprise; holidays are coming, and I'm absolutely expecting to be hit increasingly frequently with biologics. Buckle up friends. This is what they normally do.
What an odd day it has been. We had no discrete plumes today. Yes, you heard right. No discrete plumes today. Throughout the morning and afternoon, intensity wavered gently between 7.5 and 7.75+, but with no plumes.
We have a storm coming Monday. A couple weeks ago we had a no-plume-day a day or two before a big incoming storm system. Is this the reason we had a non-plume day today?
Tonight we did have a plume however. At about 6 pm intensity rose to 8.25, so this may be considered a "plume", but intensity remained there and finally began to taper off at about 9:45 pm. But that's it.
A very strange non-plume day. A one-plume night.
Intensity as I type this (12:21 am 12/10) is 8 and steady.
12:46 am (12/10)
At about 12:30 am (12/10) we were hit with a wide-spectrum plume. This plume does have low-intensity TYPE III Biologics.
The Daily Principle: Ignorance Is Deception's Invitation
When a person refuses knowledge, they refuse their own defense against deception.
We live in a time when the world teaches people to "follow your heart". This mantra is intended to cause the public to focus attention on themselves. Focus on one's self leads to ignorance of the nature and structure of the world. Such ignorance opens the door to deception.
This deception is designed to coerce the world into believing the governments of the world are not completely controlled, but rather a maelstrom of disconnected personages acting in their own interest. If the world were to realize that all governments are controlled, they would clearly see the wickedness of their coordinated actions and would eventually become actively involved in purging corruption and supporting integrity and justice.
Therefore, intentionally-promoted ignorance is specifically designed to lead the public into tolerance of the wicked actions of the governments of the world. Because the public does not know that persons in high places of governments work intimately together, the public concludes nothing can be done to stop the wars they create and profit from.
Those persons on high places conduct controlled wars profit from wars through their military contractors, and control the outcome which eventually leads to yet another ongoing - and tremendously profitable - war in the future.
Bee pollen is among the oldest known nutritional supplements, with records of its use dating back to ancient Chinese and early Egyptian medicine. Although bee pollen is gathered by honeybees as a source of nutrition for the hive, it is also used for its nutritional value in the human diet. Bee pollen is available as a dietary supplement and is regarded by many as a nutritionally-rich "perfect food."1-4
Bee pollen contains many nutrients in concentrated amounts and is a rich source of protein, carbohydrates, minerals and essential fatty acids. Bee pollen also provides B-complex vitamins and vitamin C, amino acids, trace elements and enzymes.5-8
Bee pollen is widely used in China as a food supplement and herbal tonic for enhancing the body’s resistance to disease, including cancer. In Germany, bee pollen is recommended as an appetite stimulant. Bee pollen is also commonly used to enhance energy levels and improve endurance and stamina.5,9,10
Bee pollen exhibits strong antioxidant activity and other health-protective benefits, including anti-estrogenic and bone-loss preventative effects. Animal studies have found that bee pollen provides an anabolic (building-up) action on bone components and increases bone calcium content, while in vitro studies show that bee pollen inhibits bone resorption. In addition, animal studies have shown that bee pollen improves maternal nutritional status with no adverse effects on normal fetal development, suggesting that bee pollen may be an effective nutritional supplement during pregnancy.1,4,11-13
Bee pollen has long been used as a natural remedy against allergies. A recent animal study confirmed that daily supplementation with bee pollen significantly reduced mast cell activation, thus providing an anti-allergic action. Activation of mast cells plays a pivotal role in allergic diseases. Another study determined that myricetin is one of the flavonoids in bee pollen that is responsible for its anti-allergic effect.5,14-17
Research also suggests that bee pollen may help reduce prostate size and provide anti-inflammatory effects in men with BPH (benign prostatic hyperplasia or enlarged prostate) and prostatitis. A double-blind, randomized study reported significant clinical improvement in patients with chronic prostatitis who used bee pollen, compared to those in the placebo group. In addition, a randomized, double-blind, placebo-controlled study conducted in Germany using a proprietary bee pollen extract significantly improved total symptoms, pain and quality of life in men with inflammatory chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS). Furthermore, an extract from bee pollen has been shown to induce apoptosis (cell death) in human prostate cancer cells and may be a potential treatment for prostate cancer.9,14,18-22
References: 1Nakajima, Y., et. al. "Comparison of bee products based on assays of antioxidant capacities." BMC Complementary and Alternative Medicine; 2009, 9:4. 2Wells, K.R. "Bee Pollen." Encyclopedia of Alternative Medicine. . Accessed June 2009. 3Silva, T.M., et. al. "Chemical composition, botanical evaluation and screening of radical scavenging activity of collected pollen by the stingless bees Melipona rufiventris (Uruçu-amarela)." Anais da Academia Brasileira de Ciências; 2009 Jun;81(2):173-178. 4Yamaguchi, M.. "Regulatory mechanism of food factors in bone metabolism and prevention of osteoporosis." Yakugaku Zasshi: Journal of the Pharmaceutical Society of Japan; 2006, 126(11):1117-1137. 5Fetrow, C. & Avila, J. Professional’s Handbook of Complementary & Alternative Medicines. Springhouse, PA: Springhouse Corp., 1999. 6Weiner, M. & Weiner, J. Herbs That Heal: Prescription For Herbal Healing. Mill Valley, CA: Quantum, 1994. 7Orzaez Villanueva, M.T., et. al. "The importance of bee-collected pollen in the diet: a study of its composition." International Journal of Food Sciences and Nutrition; 2002, 53(3):217-224. 8Lei H, et. al. [Supercritical CO2 extraction of fatty oils from bee pollen and its GC-MS analysis]. Zhong Yao Cai: Journal of Chinese Medicinal Materials; 2004, 27(3):177-180. 9Wu, Y.D., Lou, Y.J. "A steroid fraction of chloroform extract from bee pollen of Brassica campestris induces apoptosis in human prostate cancer PC-3 cells." Phytotherapy Research; 2007, 21(11):1087-1091. 10"Bee Pollen." Natural Standard Monograph; 2008. . Accessed June 2009. 11Campos, M.G., et. al. "Age-induced diminution of free radical scavenging capacity in bee pollens and the contribution of constituent flavonoids." Journal of Agricultural and Food Chemistry; 2003, 51(3):742-745. 12Saric', A., et. al. "Antioxidant effects of flavonoid from Croatian Cystus incanus L. rich bee pollen." Food and Chemical Toxicology; 2009, 47(3):547-554. 13Xie, Y., et. al. [Effect of bee pollen on maternal nutrition and fetal growth]. Hua Xi Yi Ke Da Xue Xue Bao; 1994, 25(4):434-437. 14Lininger Jr, S., et. al. The Natural Pharmacy, 2nd Ed. Rocklin, CA: Prima Publishing, 1999. 15Ishikawa, Y., et. al. "Inhibitory effect of honeybee-collected pollen on mast cell degranulation in vivo and in vitro." Journal of Medicinal Food; 2008, 11(1):14-20. 15He, S., Walls, A.F. "Experimental Activation of Mast Cells and Their Pharmacological Modulation." Methods in Molecular Medicine; 2008, 138:319-330. 17Medeiros, K.C., et. al. "Anti-allergic effect of bee pollen phenolic extract and myricetin in ovalbumin-sensitized mice." Journal of Ethnopharmacology; 2008, 119(1):41-46. 18Meyerowitz, S. "Will You Bee Mine? - Bee pollen for health." Better Nutrition; May 2000. . Accessed June 2009. 19Dhar, N.B., Shoskes, D.A. "New therapies in chronic prostatitis." Current Urology Reports; 2007, 8(4):313-318. 20Nickel, J.C. "The overlapping lower urinary tract symptoms of benign prostatic hyperplasia and prostatitis." Current Opinion in Urology; 2006 Jan;16(1):5-10. 21Duclos, A.J., et. al. "Current treatment options in the management of chronic prostatitis." Therapeutics and Clinical Risk Management; 2007, 3(4):507-512. 22Wagenlehner, F.M., et. al. "A Pollen Extract (Cernilton) in Patients with Inflammatory Chronic Prostatitis-Chronic Pelvic Pain Syndrome: A Multicentre, Randomized, Prospective, Double-Blind, Placebo-Controlled Phase 3 Study." European Urology; 2009, June 3. [Epub ahead of print]
The Daily Spraying Log
11:35 am
Overnight spraying was typical. Intensity ranged from7.5 to 7.75. The typical wide-spectrum mix of component were in the air dominated by the Model Cement type.
Events so far today...
We were hit with a plume before 7 am that has been layered all morning, even as I type this, and remains at intensity 8.75 right now (11:39 am).
2:08 pm - ...and again; as I was typing the entry above, we were hit with a Burnt type plume. These rise very quickly. In 2 minutes intensity can go from 0 to 9.
~2:06 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75+, Rising
10:03 pm
A lot has happened, plus, I had to run into Bangor tonight, so I will report conditions there a well. It has been a pretty brutal day overall.
Following are the events that have taken place so far this afternoon and evening.
~12:09 am (12/9) Event (home): Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.5+, Rising
What a crazy day. What crazy times.
1:30 am (12/9)
~1:20 am (12/9) Event (home): Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75, Rising
December 7 - The Daily Spraying Log Reputation-based medicine... Subscribe To My Substack - Still Free #thedailysprayinglog - #chemtrailsitswhatyoubreathe
The Daily Principle: Reputation, Not Regulation
Reputation-based medicine: If a therapy works, allow the people to use it.
Regulation, on the other hand, centralizes power and prohibits people from trying new things. Regulation is the forerunner of monopolies, far-higher pricing, and reduced quality of service.
Reputation-based commerce is God's built-in system of filtering out the bad and leaving the good.
Regulation is the centralization of power, the tower-of-Babel way of control, coercion, and a breeding ground of corruption.
Vitamin C is an important anti-stress antioxidant and vital nutrient for adrenal function. Vitamin C is more highly concentrated in the adrenal cortex than in any other organ, and when the adrenals are under stress, vitamin C levels are depleted. Experimental and clinical evidence suggests that supplemental vitamin C in levels significantly greater than the RDA (recommended dietary allowance) can support adrenal function and decrease high cortisol levels—elevated cortisol levels suppress the immune system. Likewise, animal research has shown that megadoses of vitamin C (equivalent to several thousand milligrams in humans) significantly reduces stress-hormone levels and other indicators of emotional and physical stress, including adrenal gland enlargement and changes in the thymus and spleen. Furthermore, vitamin C has been shown to improve the ability of the adrenal glands to adapt to surgical stress in lung cancer patients.1,2,4,5-8
Thiamine (vitamin B1) acts as a coenzyme in the conversion of glucose into energy. Experimental and clinical results have demonstrated the effectiveness of thiamine in protecting the adrenal glands from functional exhaustion secondary to surgery. In addition, positive results of experimental and clinical studies have shown that supplementation of thiamine in doses much higher than the RDA can support adrenal gland function. Furthermore, thiamine is essential for healthy nervous system function and has been termed the "morale vitamin“as a result of its beneficial effect on mental attitude. For example, 4 double-blind studies demonstrated an association between improved thiamine status and elevated mood, while a study of 120 young adult females found that improvement in thiamine status correlated with reports of participants being more clear-headed, composed and energetic—these results were demonstrated in participants whose thiamine status was "adequate“ according to traditional standards.2,9-11
Riboflavin (vitamin B2) is essential for endocrine health and functions as a necessary component in the metabolism of carbohydrates, fats and proteins for energy. Riboflavin also plays a role in maintaining glutathione, one of the body’s most important antioxidants. Glutathione protects the adrenal cortex against a large number of toxic chemicals. Consequently, depletion of glutathione contributes to the development of chemically-induced adrenocortical necrosis (the death of adrenal cortex cells). Thus, riboflavin deficiency can result in enhanced oxidative stress, as well as a lack of stamina and vigor, due to mitochondrial dysfunction (disrupted energy production).1,9,12-14
Vitamin B6 (pyridoxal-5-phosphate) is essential for growth and maintenance of nearly every body function. Vitamin B6 is necessary for the conversion of tyrosine (an amino acid) to dopamine, an adrenaline precursor. In addition, vitamin B6 is vital for normal adrenal function—experimental and clinical studies show that vitamin B6 supplementation in doses significantly higher than the RDA support adrenal gland function. Furthermore, vitamin B6 status significantly affects the production of neurotransmitters such as serotonin and GABA, which control anxiety, depression and pain perception. Unfortunately, human studies indicate that the bioavailability of vitamin B6 from natural food sources is limited. Vitamin B6 is converted in the liver into pyridoxal-5-phosphate (PLP), the metabolically active form of vitamin B6. Individuals with poor liver function may not be able to adequately convert "inactive“ forms of vitamin B6 (such as pyridoxine hydrochloride) into PLP.1,2,5,15-17
Pantothenic acid (vitamin B5) - A close correlation exists between tissue levels of pantothenic acid and the functioning of the adrenal cortex—animal studies show that pantothenic acid is highly retained in the adrenal tissues. Pantothenic acid participates in nerve transmissions and in the production of adrenal hormones that control the body’s reactions to emotional and physical stress and the "fight-or-flight response.“ Pantothenic acid can also improve the body’s ability to withstand stressful conditions. Based on animal and human trials, pantothenic acid supplementation is important in order to maintain adequate levels in individuals under stress—evidence indicates that adrenal cortex function is compromised when there is a deficiency of pantothenic acid derivatives and metabolites. Furthermore, pantothenic acid deficiency can lead to adrenal atrophy, characterized by mental depression, fatigue, headache, sleep disturbances, abdominal discomfort and nausea, and motor nerve dysfunction.2,7,9,16,18,19
Magnesium demonstrates a protective effect against stress-induced physiologic damage. Research has shown a negative correlation between magnesium balance and oxidative stress—chronic stress or injury reduces magnesium levels and simultaneously increases the intensity of oxidative stress upon the body. Magnesium deficiency also increases the risk of stress-induced cardiovascular damage. In addition, magnesium deficiency has been shown to impair vitamin B6 status. Furthermore, animal studies have found that magnesium deficiency decreases specific immune response and accelerates the progressive degeneration of the thymus.1,20-25
Zinc is an essential trace mineral that contributes to the normal absorption and action of vitamins, especially the B-complex vitamins. Zinc is also essential for normal functioning of the central nervous system, and plays a critical role in the health of the adrenal glands—zinc is recommended for adrenal insufficiency. Evidence suggests that zinc levels decline following physical and mental stress. For example, a study of rats showed that plasma zinc levels significantly decreased after trauma. In another animal study, dietary zinc deficiency impaired the response of brain metallothioneins (MTs)—low molecular weight proteins that regulate cellular adaptation to stress—during stress in a highly specific manner. Furthermore, zinc deficiency has been shown to increase oxidative stress; cause alterations in adrenal secretion; and impair a large number of immune functions and defense mechanisms.5,9,16,19,26-30
Potassium is an essential mineral required for proper energy metabolism and cell function. Potassium also assists with muscle contraction and transmission of nerve signals, regulates fluid and mineral balance, and facilitates kidney function. In addition, potassium is vital for normal blood pressure—decreased potassium intake may result in hypertension and heart disease. Furthermore, potassium deficiency is one of the major causes of adrenal exhaustion.16,31,32
Adrenal substance - Raw animal glandular tissues are used to nourish the corresponding human gland and support its function. Published research dating back to 1931 indicates that oral adrenal extracts have been used in medicine and have been found to be effective. Adrenal extracts provide the body with nutritional factors that can help stimulate a sluggish gland and enhance its function. Used in conjunction with supportive nutrients such as vitamin C, potassium and pantothenic acid, bovine adrenal extracts are most often recommended for low adrenal function, characterized by fatigue, inability to cope with stress, and reduced resistance to infection. Adrenal substances have been derived from certified BSE-free (Bovine Spongiform Encephalopathy-free) cows from New Zealand.1,5,16,33-35
Schizandra appears to have adaptogenic properties that enhance the body’s resistance to a variety of physical, chemical and emotional stresses, while simultaneously improving overall regulation of physiological functions. For example, schizandra has been used to combat the effects of stress and fatigue, while some scientific studies have shown that schizandra provides a normalizing effect in cases of insomnia and physical duress. Schizandra also counters the effects of caffeine and improves mental function. In addition, available data show that schizandra decreases fatigue, increases work capacity, accelerates recovery time following exercise in athletes, and enhances the hepatic (liver) glutathione antioxidant system. Furthermore, experimental evidence suggests that schizandra exhibits antibacterial activity and functions as a potent antioxidant—active constituents demonstrate strong scavenging effects against active oxygen radicals.1,36-39
Borage oil - Results from both animal and human studies suggest that borage can improve the body’s response to stress. For example, borage oil was shown to improve cardiovascular reactivity to acute stress—borage oil reduced blood pressure and heart rate responses to stress in 10 men. In a more recent animal study, borage oil lowered systolic blood pressure by inhibiting adrenal responsiveness to angiotensin II—a chemical that increases blood pressure by narrowing the arteries. In addition, borage reportedly acts as a restorative agent on the adrenal cortex.40-43
Licorice exhibits a regulatory action on the adrenal glands and appears to have an effect on every system of the body. Licorice contains the active component glycyrrhizin, which can bind to glucocorticoid receptors, thus enhancing the activity of cortisol—a steroid hormone involved in glucose control, carbohydrate/fat/protein metabolism, inflammatory regulation, and the stress response. Glycyrrhizin also suppresses 5-beta-reductase, the main enzyme responsible for inactivating both cortisol and aldosterone—a steroid hormone that regulates the body's electrolyte balance. Licorice may be most beneficial in circumstances involving prolonged stress, where the ability of the adrenal glands to respond by releasing cortisol has been diminished. Furthermore, licorice may also be helpful for adrenal corticoid abnormalities such as adrenal insufficiency, adrenal enzyme deficiency, adrenalectomy (removal of both adrenal glands) and Addison’s disease—failure of the adrenal cortex to produce aldosterone and cortisol.2,5,16,38,44
Protease blend - Proteases are enzymes that break down proteins into single amino acids. As with other proteins, raw animal glandular tissues must be digested or broken down in order to extract their nutrients. Incomplete digestion of proteins can result in a number of health problems, including the development of allergies, loss of nutrition, and the build-up of toxins in the bowel. Thus, protease enzymes facilitate the digestion of glandular substances to ensure optimal assimilation of their nutritional factors.33,45
References: 1Ronzio PhD, R.A. "Nutritional support for adrenal function.“ American Journal of Natural Medicine; 1998, 5(5):12-17. 2Kelly ND, G.S. "Nutritional and Botanical Interventions to Assist with the Adaptation to Stress.“ Alternative Medicine Review; 1999, 4(4):249-265. 3Vanitallie, T.B. "Stress: a risk factor for serious illness.“ Metabolism; 2002, 51(6 Suppl 1):40-45. 4Lavalle RPh, J.B. "Stress: The Hidden Factor For Weight Gain.“ Nutrition Science News; April 2001. 5Ghen DO, M.J. & Moore MD, C.B. "Implications of Adrenal Insufficiency.“ International Journal of Integrative Medicine; 2000, 2(6):30-35. 6Redmann, A., et. al. "Ascorbate depletion prevents aldosterone stimulation by sodium deficiency in the guinea pig.“ European Journal of Endocrinology; 1995, 133(4):499-506. 7Clute, M. "Customers On Edge? Calm Them Naturally.“ Natural Foods Merchandiser; April 2002. 8Gromova, E.G., et. al. [Regulation of the indices of neuroendocrine status in surgical patients with lung cancer using optimal doses of ascorbic acid]. Anesteziologiia I Reanimatologiia; 1990, (5):71-74. 9Dunne, L.J. Nutrition Almanac, 3rd Ed. NY, NY: McGraw-Hill Publishing Co.; 1990. 10Benton, D. & Donohoe, R.T. "The effects of nutrients on mood.“ Public Health Nutrition; 1999, 2(3A):403-409. 11Benton, D., et. al. "Thiamine supplementation mood and cognitive functioning.“ Psychopharmacology (Berl); 1997, 129(1):66-71. 12Hendler MD, S. The Doctor’s Vitamin & Mineral Encyclopedia. NY, NY: Simon & Schuster, 1990. 13Szabo, S. & Lippe, I.T. "Adrenal gland: chemically induced structural and functional changes in the cortex.“ Toxicologic Pathology; 1989, 17(2):317-329. 14Wacker, J., et. al. "Riboflavin deficiency and preeclampsia.“ Obstetrics and Gynecology.; 2000, 96(1):38-44. 15McCarty, M.F. "High-dose pyridoxine as an 'anti-stress' strategy.“ Medical Hypotheses.; 2000, 54(5):803-807. 16Pizzorno, J & Murray, M. A Textbook of Natural Medicine, 2nd ed. London: Churchill Livingstone, 1999. 17"Vitamin B6 (Pyridoxine; Pyridoxal 5’-Phosphate).“ Alternative Medicine Review; 2001, 6(1):87-92. 18Pietrzik, K. & Hornig, D. "Studies on the distribution of (1-14C) pantothenic acid in rats.“ International Journal for Vitamin and Nutrition Research; 1980, 50(3):283-293. 19Lieberman PhD, S. & Bruning, N. The Real Vitamin & Mineral Book, 2nd Ed. Avery Publ.; 1997. 20Galland, L. "Magnesium, stress and neuropsychiatric disorders.“ Magnesium and Trace Elements; 1991-92, 10(2-4):287-301. 21Cernak, I., et. al. "Alterations in magnesium and oxidative status during chronic emotional stress.“ Magnesium Research; 2000, 13(1):29-36. 22—. "Characterization of plasma magnesium concentration and oxidative stress following graded traumatic brain injury in humans.“ Journal of Neurotrauma; 2000, 17(1):53-68. 23Planells, E., et. al. "Effect of magnesium deficiency on vitamin B2 and B6 status in the rat.“ Journal of the American College of Nutrition; 1997, 16(4):352-356. 24Petrault, I., et. al. "Changes in gene expression in rat thymocytes identified by cDNA array support the occurrence of oxidative stress in early magnesium deficiency.“ Biochimica et Biophysica Acta; 2002, 1586(1):92-98. 25Malpuech-Brugere, C., et. al. "Accelerated thymus involution in magnesium-deficient rats is related to enhanced apoptosis and sensitivity to oxidative stress.“ The British Journal of Nutrition; 1999, 81(5):405-411. 26Giralt, M., et. al. "Effect of dietary zinc deficiency on brain metallothionein-I and -III mRNA levels during stress and inflammation.“ Neurochemistry international; 2000, 36(6):555-562. 27Cheng, Y., et. al. [Effects of stress on indices for assessing zinc nutrition status]. Zhonghua Yu Fang Yi Xue Za Zhi; 1996, 30(1):20-22. 28Aschner, M. "The functional significance of brain metallothioneins.“ The FASEB Journal; 1996, 10(10):1129-1136. 29Oteiza, P.I., et. al. "Zinc deficiency induces oxidative stress and AP-1 activation in 3T3 cells.“ Free Radical Biology & Medicine; 2000, 28(7):1091-1099. 30Brandao-Neto, J., et. al. "Zinc acutely and temporarily inhibits adrenal cortisol secretion in humans. A preliminary report.“ Biological Trace Element Research; 1990, 24(1):83-89. 31"FDA Grants Health Claim to Potassium.“ Nutrition Science News; January 2001. 32Treasure, J. & Ploth, D. "Role of dietary potassium in the treatment of hypertension.“ Hypertension; 1983, 5(6):864-872. 33Murray ND, M.T. Glandular Extracts. New Canaan, CT: Keats Publishing, 1994. 34Gazella, K.A. "What glandular extracts can do for you.“ Nature’s Impact; August/September 1998:8-9. 35"Glandular Therapy.“ Hayward, CA: NutriColgy, Inc., April 2003. 36"Schisandra: Structure/Function Claim.“ Nutrition Science News; January 2001. 37Sinclair ND, S. "Chinese Herbs: A Clinical Review of Astragalus, Ligusticum, and Schizandrae.“ Alternative Medicine Review; 1998, 3(5):338-344. 38May, T.G. "Adapting To Long-Term Stress.“ Natural Foods Merchandiser; April 2000. 39"Schisandra Berries More Than a Liver Aid.“ Nutrition Science News; January 2001. 40Fetrow, C. & Avila, J. Professional’s Handbook of Complementary & Alternative Medicines. Springhouse Corp., 1999. 41Mills, D.E., et. al. "Dietary fatty acid supplementation alters stress reactivity and performance in man.“ Journal of human hypertension; 1989, 3(2):111-116. 42Engler, M.M., et. al. "Effects of dietary gamma-linolenic acid on blood pressure and adrenal angiotensin receptors in hypertensive rats.“ Proceedings of the Society for Experimental Biology and Medicine; 1998, 218(3):234-237. 43Newall, C., et. al. Herbal Medicines. London, England: The Pharmaceutical Press, 1996. 44Presser PharmD, A. Pharmacist’s Guide to Medicinal Herbs. Petaluma, CA: Smart Publications, 2000. 45Cichoke DC, A.J. Enzymes & Enzyme Therapy, 2nd Ed. Los Angeles, CA: Keats Publishing, 2000.
After the final horrific plume last night just before 2 am, intensity through the rest of the night ranged between 7.5 and 7.75+. This is typical for recent history.
The sky is clear with no visible, persistent trails, but that does not mean that the trails are not being laid down. Most trails in our area are now very short, non-persistent trails and do not leave long lines in the sky. You can read more about how and why this changed here:
~2:15 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.5. Rising
2:37 pm
We are getting hit with a wide-spectrum plumes that contains TYPE III Biologics:
~2:25 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Type III Biologics - This type makes your body hurt like you have the flu but without a fever. - Chalky-Bitter-Pharma - Stimulant - Inflammatory - Mercury Intensity Delta: Medium-Fast Current Intensity: 9.25, Rising
10:30 pm
I had a talk show tonight I am late posting these events.
It's been a pretty "normal" night of poisoning except for the last plume at 7:48 pm. This plume was very intense and happened while the show was happening. I still have the headache that this plume gave me.
~3:48 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 8.75
~6:04 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Type III Biologics - This type makes your body hurt like you have the flu but without a fever. - Chalky-Bitter-Pharma - Stimulant - Inflammatory - Mercury Intensity Delta: Medium-Fast Peak Intensity: 9.5
~6:10 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Type III Biologics - This type makes your body hurt like you have the flu but without a fever. - Chalky-Bitter-Pharma - Stimulant - Inflammatory - Mercury Intensity Delta: Medium-Fast Peak Intensity: 10
~6:34 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 9.25
~7:48 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Type III Biologics - This type makes your body hurt like you have the flu but without a fever. - Copper - This plume had the Copper type, which we have not had for a while. This type really induces headaches in both of us. - Chalky-Bitter-Pharma - Stimulant - Inflammatory - Mercury Intensity Delta: Medium-Fast Peak Intensity: 10
This last type is still in the air 2 1/2 hours later. It's not strong right now, but it reall has lingered a long time.
Intensity right now is 8- with the Model Cement and Copper types still lingering from the previous plume. What a horrible plume this was.
10:58 pm
We often get hit at 11 pm, and so this is "that" plume.
~11:10 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.75 - This rose very fast.
12:42 am (12/8)
Here is out nightly 12:30 am plume.
~12:30 am (12/8) Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Chalky-Bitter-Pharma - Stimulant - Inflammatory - Mercury Intensity Delta: Medium-Fast Current Intensity: 8.5-
1:02 am (12/8)
~12:55 am (12/8) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75, Rising
December 6 - The Daily Spraying Log - Probiotic Types
Overnight
After the final horrendous plume hit us at 2:12 am this morning, we had no new plumes until about 10:50 am this morning. The average intensity through the night was between 7.5- and 7.25+. A little lower than usual.
Today, we have been hit with 3 plumes so far. All of been identical in composition, but different in intensity.
Just a few links that are critical for understanding how the world works.
Many are waking up, but so many are still avoiding knowledge like the plague, even though this is the worst time in history for one to be willfully ignorant.
Please share this page/newsletter with those you care about to help them learn truth and keep them safe from making dangerous, uneducated decisions in this perilous time we live in.
If you still haven't seen it, this is a must-watch video for understanding why the world is going the way it is. Share it far and wide:
Probiotics are defined as live microorganisms that, once ingested, demonstrate a beneficial effect upon the body by improving the balance of the intestinal flora. The most reliable and well-researched probiotic organisms belong to either the lactobacillus or bifidobacteria genera—lactobacillus bacteria reside mainly in the small intestine and bifidobacteria colonize the large intestine. Probiotics inhibit the growth of harmful microorganisms, boost immune function, increase resistance to infection and promote healthy digestion. However, antibiotic use and alcohol, as well as disease and aging, can disrupt the balance of intestinal microflora, thus negatively affecting the beneficial role these important microorganisms play.1-6
Much of the research on probiotics has focused on diarrhea prevention and intestinal health, stomach ulcers, immunity and women's urogenital health. However, promising data also exists on the use of probiotics for combating Helicobacter pylori stomach infections, modulating mucosal immunity (the first line of defense against foreign invaders), reducing the risk of certain cancers, minimizing surgical complications, and decreasing serum cholesterol and oxaluria—the excess of calcium oxalate in the urine, which contributes to the formation of kidney stones. Furthermore, preliminary human studies suggest that probiotics have a positive effect in the treatment of colitis (inflammation of the colon), also known as irritable bowel disease (IBD)—a general term for a group of diseases involving intestinal-wall inflammation and characterized by recurrent crampy abdominal pain and diarrhea, including Crohn's disease and ulcerative colitis.1,4-11
Lactobacillus rhamnosus has been shown to enhance systemic cellular immune responses in healthy volunteers. Studies have found that L. rhamnosus also alleviates clinical symptoms of gastrointestinal inflammation and atopic dermatitis, and significantly reduces the occurrence of atopic eczema (an inflammatory skin condition characterized by redness, itching and oozing lesions that become scaly, crusted or hardened) in children. In addition, two separate studies involving children (ages 1 to 36 months) showed that L. rhamnosus significantly shortened the duration of acute-onset rotavirus diarrhea compared to placebo. Furthermore, a one-month trial involving 10 infants with food-allergy-related dermatitis showed that L. rhamnosus provided significant clinical improvements in the infants’ conditions, compared to those given a placebo.4,5,12-19
Bifidobacterium bifidum is among the most widely used and studied probiotic bacteria, with numerous therapeutic effects demonstrated in clinical studies, including eczema in infants and irritable bowel syndrome in adults. Use of B. bifidum in combination with other probiotics (S. thermophilus and L. rhamnosus) has also been proven effective in the treatment of Clostridium difficile—a potentially fatal bacterial infection that causes severe diarrhea. In addition, a recent six-week randomized, double-blind, placebo-controlled study also found that B. bifidum reduced stress-related diarrhea symptoms in undergraduate students taking final exams.20-23
Lactobacillus acidophilus has demonstrated significant antioxidant activity and has been shown to prevent several intestinal pathogens (disease-causing microorganisms) from attaching to human intestinal cells, including Escherichia coli, Yersinia pseudotuberculosis and Salmonella typhimurium. L. acidophilus also inhibits the growth of Helicobacter pylori and has been proven effective in reducing the duration of acute diarrhea in children. In addition, L. acidophilusis regarded as a successful natural treatment for bacterial vaginosis (vaginal infection), particularly in pregnant women, due to the lack of systemic side effects. Furthermore, a controlled clinical study found that L. acidophilus can reduce serum cholesterol and thus, demonstrates the potential for reducing the risk of coronary heart disease.9,24-30
Lactobacillus brevis has been shown to alter the immunological responses in humans. For example, a study found that oral intake of L. brevis significantly increased the interferon-alpha (IFN-alpha) producing capacity of apparently healthy subjects and was especially beneficial in those with initially low levels of IFN-alpha production—IFN-alpha is a protein that exhibits pronounced antiviral activity and causes the activation of natural killer cells. Other research has shown that L. brevis inhibits the activity of potentially harmful microorganisms, including Bacillus cereus—a bacteria that causes food poisoning. L. brevis has also been shown to efficiently induce apoptosis (programmed cell death) in vitro in Jurkat cells—human T-leukemia cells that are used to test the effects of anticancer drugs and radiation.31-33
Lactobacillus bulgaricus has demonstrated strong immunopotentiating activity and has been shown to induce significant increases in interleukin-6 (IL-6) production by macrophages—IL-6 is a protein that stimulates the growth and differentiation of human B-cells (a type of white blood cell that fights viral infections). L. bulgaricus has also been shown to significantly inhibit intestinal carcinogenesis (the formation of cancer) in rats by decreasing the occurrence and number of tumors. In addition, two double-blind controlled studies have confirmed the effectiveness of L. acidophilus and L. bulgaricus against antibiotic-associated diarrhea.34-37
Lactobacillus plantarum appears to be an effective treatment for irritable bowel syndrome (IBS), as demonstrated by its ability to reduce flatulence (gas) and abdominal pain. In addition, a double-blind study found that L. plantarum significantly reduced fibrinogen—a suspected independent risk factor for thrombosis—and LDL-cholesterol concentrations in serum of men with moderately elevated cholesterol. A follow-up controlled, randomized, double-blind trial determined that L. plantarum intake also led to a decrease in cardiovascular disease risk factors, including significant reductions in systolic blood pressure, and thus, could be useful in the prevention of atherosclerosis in smokers. Furthermore, L. plantarum has been shown to minimize surgical complications, including post-operative infections.4,18,38-42
Streptococcus thermophilus, a beneficial bacteria frequently found in yogurt, exhibits antioxidant activity and the ability to inhibit the oxidation of low-density lipoproteins (LDL). S. thermophilus has also demonstrated iron-chelating abilities. In addition, S. thermophilus exhibited antitumor activity in mice and reduced the incidence of large, chemically-induced intestinal tumors in rats. Furthermore, the intake of yogurt fermented with Lactobacillus bulgaricus and S. thermophilus produced a clinically relevant decrease in stool frequency and duration of acute diarrhea in children.5,43-47
Bifidobacterium infantis has shown antimicrobial activity against Clostridium difficile—one of the most common causes of infection of the colon. B. infantis has also been shown to greatly inhibit the growth of Bacteroides vulgatus in mice—B. vulgatus is a bacteria that may be responsible for, or at least contribute to, the development of inflammatory bowel disease (IBD). In addition, a prospective clinical study found the oral intake of L. acidophilus and B. infantis statistically improved the frequency of diarrhea in children with acute diarrhea on the first and second day of treatment, as well as decreased the duration of diarrhea.48-51
Bifidobacterium longum exhibited protective effects against invasion of the intestinal mucosa by dietary antigens, as well as significantly suppressed colon tumor incidence in animal studies. B. longum has also demonstrated significant antioxidant activity. In addition, a randomized, double-blind trial found that B. longum improved lactose digestion in 15 lactose malabsorbers, as evidenced by reduced symptoms of flatulence. Furthermore, a study involving 32 patients with borderline to high cholesterol showed that B. longum reduced total cholesterol in approximately 50% of treated patients, with significant decreases among those with total cholesterol levels greater than 240 mg/dl.20,52-55
Lactobacillus casei significantly increased natural killer (NK) cell activity in healthy volunteers, particularly those exhibiting low NK activity. In addition, a controlled pilot study showed that L. casei reduced the duration of winter infections (gastrointestinal and respiratory) by 20% in elderly people. Furthermore, a 4-month double-blind, randomized trial involving 928 children (ages 6 to 24 months) found that L. casei significantly reduced the frequency of diarrhea.56-58
Lactobacillus salivarius completely inhibited the growth of Helicobacter pylori (H. pylori) in vitro and also suppressed H. pylori and reduced the associated inflammatory response in vivo. In addition, a placebo-controlled trial found that L. salivarius intake was associated with reduced prevalence of colon cancer and mucosal inflammatory activity in mice. Furthermore, both L. brevis and L. salivarius exhibited properties that researchers found would make them good alternatives to antibiotics for the probiotic prophylaxis (prevention) and treatment of human vaginal infections, including their ability to adhere to epithelial cells and displace vaginal pathogens; their production of high levels of hydrogen peroxide (H2O2), which makes the intestinal pH more acidic and thus, inhospitable for pathogens; and their ability to inhibit the growth of Gardnerella vaginalis, which is implicated in the cause of bacterial vaginosis—a vaginal infection characterized by excessive, sometimes unpleasant-smelling discharge.59-61
Fructooligosaccharides are a type of nondigestible fiber, derived from foods such as asparagus, garlic, Jerusalem artichoke and onion, that can be considered a prebiotic—a nutritional substance that stimulates the growth of probiotic organisms, leading to a beneficial balance of healthy and harmful intestinal flora. FOS specifically stimulate bifidobacteria growth, while suppressing the growth of potentially harmful pathogens such as Clostridium perfringens (a common infectious cause of outbreaks of food-borne illness) in the colon. In addition, FOS enhance magnesium absorption in humans and have been shown to reduce colon tumor development in animal studies.5,9,62-68
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"Probiotics in primary prevention of atopic disease: a randomised placebo-controlled trial." Lancet; 2001, 357(9262):1076-1079. 16Shornikova, A.V., et. al. "A trial in the Karelian Republic of oral rehydration and Lactobacillus GG for treatment of acute diarrhoea." Acta Paediatrica; 1997, 86(5):460-465. 17Guandalini, S., et al. "Lactobacillus GG administered in oral rehydration solution to children with acute diarrhea: a multicenter European trial." Journal of Pediatric Gastroenterology and Nutrition; 2000, 30:54-60. 18Reid PhD, G. "Beneficial Bacteria." Natural Foods Merchandiser; April 2003. 19Majamaa, H., et al. "Probiotics: a novel approach in the management of food allergy." Journal of Allergy and Clinical Immunology; 1997, 99(2):179-185. 20Ku, S., et. al. "Review on Bifidobacterium bifidum BGN4: Functionality and Nutraceutical Applications as a Probiotic Microorganism.” International Journal of Molecular Sciences; 2016, 17(9). 21Gargari, G., et. al. 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"The bactericidal effects of Lactobacillus acidophilus, garcinol and Protykin compared to clarithromycin, on Helicobacter pylori." Molecular and Cellular Biochemistry; 2003, 243(1-2):29-35. 27Vilaichone, R.K., et. al. "Inhibitory effect of Lactobacillus acidophilus on Helicobacter pylori in peptic ulcer patients: in vitro study." Journal of the Medical Association of Thailand; 2002, 85 Suppl 1:S79-84. 28Simakachorn, N., et. al. "Clinical evaluation of the addition of lyophilized, heat-killed Lactobacillus acidophilus LB to oral rehydration therapy in the treatment of acute diarrhea in children." Journal of Pediatric Gastroenterology and Nutrition; 2000, 30(1):68-72. 29Andreeva, P. & Dimitrov, A. [The probiotic Lactobacillus acidophilus—an alternative treatment of bacterial vaginosis]. Akusherstvo i Ginekologiia (Sofiia); 2002, 41(6):29-31. 30Anderson, J.W. & Gilliland, S.E. "Effect of fermented milk (yogurt) containing Lactobacillus acidophilus L1 on serum cholesterol in hypercholesterolemic humans." Journal of the American College of Nutrition; 1999, 18(1):43-50. 31Kishi, A., et. al. "Effect of the oral administration of Lactobacillus brevis subsp. coagulans on interferon-alpha producing capacity in humans." Journal of the American College of Nutrition; 1996, 15(4):408-412. 32Ronka, E., et. al. "Probiotic and milk technological properties of Lactobacillus brevis." International Journal of Food Microbiology; 2003, 83(1):63-74. 33Di Marzio, L., et. al. "Apoptotic effects of selected strains of lactic acid bacteria on a human T leukemia cell line are associated with bacterial arginine deiminase and/or sphingomyelinase activities." Nutrition and Cancer; 2001, 40(2):185-196. 34Nagafuchi, S., et. al. "Strain dependency of the immunopotentiating activity of Lactobacillus delbrueckii subsp. bulgaricus." Bioscience, Biotechnology, and Biochemistry; 1999, 63(3):474-479. 35Marin, M.L., et. al. "Stimulation of cytokine production in clonal macrophage and T-cell models by Streptococcus thermophilus: comparison with Bifidobacterium sp. and Lactobacillus bulgaricus." Journal of Food Protection; 1998, 61(7):859-864. 36Balansky, R., et. al. "Inhibitory effects of freeze-dried milk fermented by selected Lactobacillus bulgaricus strains on carcinogenesis induced by 1,2-dimethylhydrazine in rats and by diethylnitrosamine in hamsters." Cancer Letters; 1999, 147(1-2):125-137. 37Cremonini, F., et. al. "Probiotics in antibiotic-associated diarrhoea." Digestive and Liver Disease; 2002, 34 Suppl 2:S78-80. 38Nobaek, S., et. al. "Alteration of intestinal microflora is associated with reduction in abdominal bloating and pain in patients with irritable bowel syndrome." American Journal of Gastroenterology; 2000, 95(5):1231-1238. 39Podell MD, R.N. "New Lactobacillus Strains Need Research." Nutrition Science News; November 2001 40Niedzielin, K., et. al. "A controlled, double-blind, randomized study on the efficacy of Lactobacillus plantarum 299V in patients with irritable bowel syndrome." European Journal of Gastroenterology & Hepatology; 2001, 13(10):1143-1147. 41Bukowska, H., et. al. "Significant decrease in fibrinogen and LDL cholesterol levels upon supplementation of the diet with Lactobacillus plantarum (ProViva) in subjects with moderately elevated cholesterol concentrations." Atherosclerosis; 1998, 137:437–438. 42Naruszewicz, M., et. al. "Effect of Lactobacillus plantarum 299v on cardiovascular disease risk factors in smokers." American Journal of Clinical Nutrition; 2002, 76(6):1249-1255. 43Terahara, M., et. al. "Prevention by lactic acid bacteria of the oxidation of human LDL." Bioscience, Biotechnology, and Biochemistry; 2001, 65(8):1864-1868. 44Lin, M.Y., et. al. "Antioxidative ability of lactic acid bacteria." Journal of Agricultural and Food Chemistry; 1999, 47(4):1460-1466. 45Kaklij, G.S., et. al. "Antitumor activity of Streptococcus thermophilus against fibrosarcoma: role of T-cells." Cancer Letters; 1991, 56(1):37-43. 46McIntosh, G.H., et. al. "A probiotic strain of L. acidophilus reduces DMH-induced large intestinal tumors in male Sprague-Dawley rats." Nutrition and Cancer; 1999, 35(2):153-159. 47Boudraa, G., et. al. "Effect of feeding yogurt versus milk in children with acute diarrhea and carbohydrate malabsorption." Journal of Pediatric Gastroenterology and Nutrition; 2001, 33(3):307-313. 48Lee, Y.J., et. al. "Identification and screening for antimicrobial activity against Clostridium difficile of Bifidobacterium and Lactobacillus species isolated from healthy infant faeces." International Journal of Antimicrobial Agents; 2003, 21(4):340-346. 49Shiba, T., et. al. "The suppressive effect of bifidobacteria on Bacteroides vulgatus, a putative pathogenic microbe in inflammatory bowel disease." Microbiology and Immunology; 2003, 47(6):371-378. 50Hashimoto, M., et. al. "Structural study on lipid A and the O-specific polysaccharide of the lipopolysaccharide from a clinical isolate of Bacteroides vulgatus from a patient with Crohn's disease." European Journal of Biochemistry; 2002, 269(15):3715-3721. 51Lee, M.C., et. al. "Oral bacterial therapy promotes recovery from acute diarrhea in children." Acta Paediatrica Taiwanica; 2001, 42(5):301-305. 52Takahashi, T., et. al. "Effects of orally ingested Bifidobacterium longum on the mucosal IgA response of mice to dietary antigens." Bioscience, Biotechnology, and Biochemistry; 1998, 62(1):10-15. 53Singh, J., et. al. "Bifidobacterium longum, a lactic acid-producing intestinal bacterium inhibits colon cancer and modulates the intermediate biomarkers of colon carcinogenesis." Carcinogenesis; 1997, 18(4):833-841. 54Jiang, T., et. al. "Improvement of lactose digestion in humans by ingestion of unfermented milk containing Bifidobacterium longum." Journal of Dairy Research; 1996, 79(5):750-757. 55Xiao, J.Z., et. al. "Effects of milk products fermented by Bifidobacterium longum on blood lipids in rats and healthy adult male volunteers." Journal of Dairy Research; 2003, 86(7):2452-2461. 56Nagao, F., et. al. "Effects of a fermented milk drink containing Lactobacillus casei strain Shirota on the immune system in healthy human subjects." Bioscience, Biotechnology, and Biochemistry; 2000, 64(12):2706-2708. 57Turchet, P., et. al. "Effect of fermented milk containing the probiotic Lactobacillus casei DN-114001 on winter infections in free-living elderly subjects: a randomised, controlled pilot study." Journal of Nutrition, Health & Aging; 2003, 7(2):75-77. 58Pedone, C.A., et. al. "Multicentric study of the effect of milk fermented by Lactobacillus casei on the incidence of diarrhoea." International Journal of Clinical Practice; 2000, 54(9):568-571. 59Aiba, Y., et. al. "Lactic acid-mediated suppression of Helicobacter pylori by the oral administration of Lactobacillus salivarius as a probiotic in a gnotobiotic murine model." American Journal of Gastroenterology; 1998, 93(11):2097-2101. 60O'Mahony, L., et. al. "Probiotic impact on microbial flora, inflammation and tumour development in IL-10 knockout mice." Alimentary Pharmacology & Therapeutics; 2001, 15(8):1219-1225. 61Mastromarino, P., et. al. "Characterization and selection of vaginal Lactobacillus strains for the preparation of vaginal tablets." Journal of Applied Microbiology; 2002, 93(5):884-893. 62Almada BSc, A. "Appliance Of Science." Functional Foods & Nutraceuticals; December 2002. 63Gibson, G.R. & Roberfroid, M.B. "Dietary modulation of the human colonic microbiota: introducing the concept of prebiotics." Journal of Nutrition; 1995, 125(6):1401-1412. 64Buddington, R.K., et. al. "Dietary supplement of neosugar alters the fecal flora and decreases activities of some reductive enzymes in human subjects." American Journal of Clinical Nutrition; 1996, 63(5):709-716. 65Reid PhD, G. "Prebiotic Plethora Colonises The Field." Functional Foods & Nutraceuticals; November 2002. 66Bouhnik, Y., et. al. "Short-chain fructo-oligosaccharide administration dose-dependently increases fecal bifidobacteria in healthy humans." Journal of Nutrition; 1999, 129(1):113-116. 67Tahiri, M., et. al. "Five-week intake of short-chain fructo-oligosaccharides increases intestinal absorption and status of magnesium in postmenopausal women." Journal of Bone and Mineral Research; 2001, 16(11):2152-2160. 68Bornet, F.R., et. al. "Nutritional aspects of short-chain fructooligosaccharides: natural occurrence, chemistry, physiology and health implications." Digestive and Liver Disease; 2002, 34 Suppl 2:S111-120.
The Daily Spraying Log - Continued
2:27 pm
They are starting the burnt type early today.
~2:20 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9, Rising
~4:20 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.25, Rising
5:22 pm
Yes! They do spray biologics that induce the flu. They have been doing this in our area since 2009. I first reported it at that time.
I am not the only one who smells and tastes biologics and the other horrible things they spray. Below is a post today from a super nice guy that I had a long conversation with some time ago. He posted this today:
For those who still have trouble believing, this is absolutely happening and those of us who smell and taste it have been telling people for years.
Here is an article I wrote about how they induced the huge flu outbreak of 2018. Please read and share it. Help get the truth out about what is being done to all of us.
~7 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9, Rising
11:37 pm
We have been hit with a Burnt type plume, however, this was a partial hit and didn't last long. This occurs when the descending plume is partly past us horizontally when it reaches ground level.
~11:14 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 8+ This didn't get very strong compared other times.
The air has now fallen to intensity 7.5- and it feels good. Some of the inflammation I live with from the spraying has declined and it feels very good. This is how I should feel all the time. But even as I'm typing this, intensity is increasing. This may be our nightly 11:30 pm hit landing on us.
What a time we live in.
11:51 pm
The rising intensity in the previous post was definitely another hit. Following is the event profile:
The intensity of the previous wide-spectrum plume is now 9.75- and still rising.
We have now been hit with a Burnt type plume.
~11:55 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9, Rising
2:02 am (12/7)
We have now been hit with another Burnt type plume. This pattern occurs nearly every night.
~1:55 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9+, Rising
December 5 - The Daily Spraying Log
They Lied About Efficacy: Here Are The Facts
Everyone globally was intentionally deceived into believing that 95% efficacy meant that they had a 95% percent reduction in risk, but nothing could be further from the truth.
Candida albicans, an opportunistic fungal pathogen (disease-causing organism) present in healthy gastrointestinal tracts, is a normal component of the human gut microbiota. Emerging data suggest that C. albicans can modulate the gut-brain axis, thus affecting human health and disease. While C. albicans normally co-exists harmlessly, increased colonization, often induced through antibiotic use, can lead to a variety of Candida infections ranging from superficial mucosal and dermal (skin) infections such as diaper rash, thrush and vaginal infections to more serious and even fatal infections. Gut dysbiosis with increased C. albicans is also associated with inflammatory bowel diseases (e.g. Crohn’s, ulcerative colitis). Plus, it is well-established that C. albicans is the primary cause of hospital-acquired infections. In addition to antibiotic use, research confirms that diet also impacts the gut microbiota. Human diets high in carbohydrates, including plant-based diets, are associated with increased Candida levels compared to animal-based diets that are rich in protein, fatty acids and amino acids.1-6
Caprylic acid is a naturally occurring fatty acid derived from coconut oil. Fatty acids demonstrate potent antimicrobial properties with broad spectrum activity against pathogens. Caprylic acid has been recommended as a dietary supplement to suppress the growth of C. albicans within the gut. Caprylic acid’s antifungal activity has been shown to inhibit the virulence factors of C. albicans (i.e. the mechanisms by which Candida causes disease). Research has shown that caprylic acid causes considerable damage to the protective cell membranes of C. albicans. In addition, by increasing cell membrane permeability, caprylic acid can help accelerate the uptake and improve the anti-Candida efficiency of other naturally-derived antimicrobials.2,3,7-12
Elecampane root (Inula helenium) has a history of traditional use in many countries for respiratory and digestive problems, inflammatory diseases, and as an insect repellent and antiparasitic agent (a substance that kills parasitic fungi, intestinal worms, and other parasitic microorganisms). Research has shown that elecampane is a rich source of active compounds known as sesquiterpene lactones that demonstrate antifungal, antibacterial, anti-inflammatory, antioxidant, and anti-helminthic (intestinal worm-killing) properties. These active compounds also exhibit strong anti-Candida activity, as well as the ability to activate cellular defense mechanisms and detoxifying enzymes.13-23
Black walnut hulls (Juglans nigra) have historically been used to treat pain and inflammation, itching skin conditions, respiratory problems, and gastrointestinal disorders such as ulcers, parasites and intestinal worms. Extracts of black walnut have demonstrated positive antifungal activity against multiple strains of Candida in vitro. Pharmacological studies have shown that juglone, an active constituent in black walnut, exhibits antifungal, antibacterial, antiviral, antiparasitic and antioxidant properties. Animal studies have shown juglone’s antifungal activity to be comparable to commercial medications used to treat athlete’s foot and ringworm. Furthermore, juglone has been shown to prevent the growth of Helicobacter pylori, a bacterium that can cause gastritis and peptic ulcers in humans.24-33
Red raspberry leaf (Rubus idaeus) - Red raspberry leaves have traditionally been used to treat inflammation and infections, including common colds, fevers and flu-like infections, as well as gastrointestinal tract ailments and colic pain. The European Medicines Agency (EMA) has approved red raspberry leaf for symptoms of mild inflammation, as well as mild diarrhea. Red raspberry leaves are a rich source of antioxidants, and active compounds with anti-inflammatory, antimicrobial, anticancer, and muscle-relaxant properties. Red raspberry leaf extracts have also been shown to have growth-promoting (e.g. prebiotic) effects on the intestinal microbiota.34-43
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[Inhibition of Candida mycelia growth by a medium chain fatty acids, capric acid in vitro and its therapeutic efficacy in murine oral candidiasis]. Medical Mycology Journal; 2012, 53(4):255-261. 12Kim, S.A., Rhee, M.S. “Use of caprylic acid to control pathogens (Escherichia coli O157:H7 and Salmonella enterica serovar Typhimurium) in apple juice at mild heat temperature.” Journal of Applied Microbiology; 2015, 119(5):1317-1323. 13Chun, J., et. al. “Sesquiterpene lactones-enriched fraction of Inula helenium L. induces apoptosis through inhibition of signal transducers and activators of transcription 3 signaling pathway in MDA-MB-231 breast cancer cells.” Phytotherapy Research; 2018, 32(12):2501-2509. 14Jiang, Y., et. al. “Alantolactone induces apoptosis of human cervical cancer cells via reactive oxygen species generation, glutathione depletion and inhibition of the Bcl-2/Bax signaling pathway.” Oncology Letters; 2016, 11(6):4203-4207. 15Mazzio, E.A., et. al. “Natural product HTP screening for attenuation of cytokine-induced neutrophil chemo attractants (CINCs) and NO2- in LPS/IFN? activated glioma cells.” Journal of Neuroimmunology; 2017, 302:10-19. 16Zlatic, N., et. al. “Temporal, Plant Part, and Interpopulation Variability of Secondary Metabolites and Antioxidant Activity of Inula helenium L.” Plants (Basel); 2019, 8(6). pii: E179. 17Lee, K.M., et. al. “Igalan induces detoxifying enzymes mediated by the Nrf2 pathway in HepG2 cells.” Journal of Biochemical and Molecular Toxicology; 2019, 33(5):e22297. 18El Garhy, M.F., Mahmoud, L.H." 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(Review).” Drug Development & Registration; 2019, 8(3):21-28. 27Abedi, P., et. al. “Comparison of the Effects of Juglans nigra Green Husk and Clotrimazole on Candida albicans in Rats.” Jundishapur Journal of Microbiology; 2018, 11 (2); e58151. 28Heisey, R.M., Gorham, B.K. "Antimicrobial effects of plant extracts on Streptococcus mutans, Candida albicans, Trichophyton rubrum and other micro-organisms." Letters in Applied Microbiology; 2008, 14(4):136-139. 29Vardhini, S.R. “Exploring the antiviral activity of juglone by computational method.” Journal of Receptors and Signal Transduction; 2014, 34(6):456-457. 30Malekzadeh, S., et. al. “Identification and Evaluation of Novel Drug Targets against the Human Fungal Pathogen Aspergillus fumigatus with Elaboration on the Possible Role of RNA-Binding Protein.” Iranian Biomedical Journal; 2017, 21(2):84-93. 31Liu, X., et. al. “Juglone potentiates TRAIL-induced apoptosis in human melanoma cells via activating the ROS-p38-p53 pathway.” Molecular Medicine Reports; 2017, 16(6):9645-9651. 32Wenzel, J., et. al. “Antioxidant potential of Juglans nigra, black walnut, husks extracted using supercritical carbon dioxide with an ethanol modifier.” Food Science & Nutrition; 2016, 5(2):223-232. 33Benites, J., et. al. “In Vitro Inhibition of Helicobacter pylori Growth by Redox Cycling Phenylaminojuglones.” Oxidative Medicine and Cellular Longevity; 2018:1618051. 34Dudzinska, D., et. al. “CD39/NTPDase-1 expression and activity in human umbilical vein endothelial cells are differentially regulated by leaf extracts from Rubus caesius and Rubus idaeus.” Cellular & Molecular Biology Letters; 2014, 19(3):361-380. 35Krauze-Baranowska, M., et. al. “Chemical composition and biological activity of Rubus idaeus shoots--a traditional herbal remedy of Eastern Europe.” BMC Complementary and Alternative Medicine; 2014, 14:480. 36Ponder, A., Hallmann, E. “Phenolics and Carotenoid Contents in the Leaves of Different Organic and Conventional Raspberry (Rubus idaeus L.) Cultivars and Their In Vitro Activity.” Antioxidants (Basel); 2019, 8(10). pii: E458. 37Ferlemi, A.V., Lamari, F.N. “Berry Leaves: An Alternative Source of Bioactive Natural Products of Nutritional and Medicinal Value.” Antioxidants (Basel); 2016, 5(2). pii: E17. 38Rojas-Vera, J., et. al. "Relaxant activity of raspberry (Rubus idaeus) leaf extract in guinea-pig ileum in vitro." Phytotherapy Research; 2002, 16(7):665-668. 39Chwil, M., Kostryco, M.” Histochemical assays of secretory trichomes and the structure and content of mineral nutrients in Rubus idaeus L. leaves.” Protoplasma; 2019, August 9. [Epub ahead of print]. 40Zielonka-Brzezicka, J., et. al. [Comparison of the antioxidant properties of selected parts of raspberry (Rubus idaeus) and blackberry (Rubus fruticosus)] Pomeranian Journal of Life Sciences; 2016, 62(4):52-59. 41Durgo, K., et. al. “The bioactive potential of red raspberry (Rubus idaeus L.) leaves in exhibiting cytotoxic and cytoprotective activity on human laryngeal carcinoma and colon adenocarcinoma.” Journal of Medicinal Food; 2012, 15(3):258-268. 42Piwowarski, J., et. al. “Role of human gut microbiota metabolism in the anti-inflammatory effect of traditionally used ellagitannin-rich plant materials.” Journal of Ethnopharmacology; 2014, 155(1):801-809. 43Kawabata, K., et. al. “Role of Intestinal Microbiota in the Bioavailability and Physiological Functions of Dietary Polyphenols.” Molecules; 2019, 24(2). pii: E370.
The Daily Spraying log
Overnight
Air intensity through the night hovered between an ambient level of 7.5 and 7.75. So even though we were hit late into the night with strong plumes (see yesterdays' log), after the last recorded plume, things fell back to ambient levels until about 7:30 am this morning.
The mix through the night was the typical wide-spectrum mix of:
~5:25 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9, Rising
8:06 pm
The air has been layered all afternoon and so we have had no real breaks. Air intensity has not fallen back to ambient levels.
Now, we have been hit with another wide-spectrum plume. This formula is different from the ones they have used all day. This one has the Sharp Metallic type as the dominant component. The Inflammatory component is next.
We had a long break where intensity fell to about 7.5 (ambient) for hours, but at 11:30 pm, we were hit with a plume, then again at 12 m, and now we've been hit again at about 12:50 am (12/6). This is a conventional, wide-spectrum plume that is the most common combination we have in recent history.
~1:20 am (12/6) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 10
2:22 am (12/6)
We are being hit with another Burnt type plume. The air is absolutely horrible.
~2:12 am (12/6) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 8.75, Rising
December 4 - The Day Everything Changed and No One Knew Why
After the onslaught of spraying/poisoning we had last night, from 3 am on, we then had one to the mildest nights of spraying we have had in a long time. The intensity of the air dropped to 7.25 and remained in that vicinity the entire night.
I just got off the phone with a friend from another part of the northeast U.S. and they had the best night of sleep they have had in a long time. Since they cannot smell or taste the spraying in the air, they attribute it others things, sadly.
Did you have a better-than-normal night of sleep last night?
I do not know if the mild night of spraying occurred throughout the entire U.S., but when getting feedback from others in the northeast, it seems that the entire northeast does experience the same general type and intensity of spraying on any given day. I draw this hypothesis based on years of feedback from others.
Certainly there are exceptions, such as weather systems that are being "worked". Because there is an independent weather-related spraying program, a part of the northeast may be affected by that spray program when the rest of the northeast is not, but generally speaking, there is a mean (average) uniformity of intensity and type in the northeast, if not beyond.
The Effect On People
It was around about 2017 when we experienced the mildest night of spraying we have had since spraying began (in our area) in 2005. Intensity dropped to about 3 to 4 overnight. This was so low that it produced no real physical affects or inflammation. I woke up feeling much better than I had in years.
At this time I had been attending the same Church for about a year, and let me tell you, that Sunday morning was so different than any other before or since; so completely different.
People we so lively, happy, alert, bright-faced, and active that is was blatantly noticeable. Now this is a great group of people; always friendly and warm, but they aren't always lively and alert. Like so much of the public that I experience, you can see the fatigue, tiredness, dark circles, and inflammation in there faces; super friendly and nice, but still tired and fatigued like the rest of us.
This particular morning however, was completely different. There was so much friendly talk and fellowship that the pastor had to ask several times to start the service before people stopped visiting with each other, but that was just the beginning.
In this church, worship takes place before the sermon. Historically, when a song is sung, there is silence afterward. During this time, people are still and contemplative. This is how it always has been, but this one particular morning was completely different, and it was the only morning since then that I have experienced this...
When a song was finished, the entire congregation clapped and cheered and showed a level of life that was beyond anything I have ever seen from them. It was so completely, absolutely different from any other Sunday morning I had experienced there. The clapping and cheering and outpouring of joy was overflowing after every single song. I cannot express how completely different it was from any other morning I have experienced there. The whole atmosphere was different; so much better.
After the service, people hung out and talked for so long and with such life... more than I have ever seen there. Yes, they are always nice and friendly and warm, but this was something far beyond that. The smiles wrapped every face. People looked younger and had more energy than I had ever seen. The pastor was also much more full of life and energy, and he witnessed the change in the congregation that morning as well.
The following week, everything returned to normal: Nice, friendly, warm, cordial. The members were all the wonderful things they always are on Sunday morning, but that environment was nothing like the explosive joy and energy and enthusiasm that I witnessed that one day; the day after a night of virtually clear air, air with almost no chemtrail fallout. I felt amazing that day and so did everyone else, and that was clearly apparent to everyone. It was such an event that I remember it to this day.
This is how it should be every day. If the poisonous spraying stopped and the induced toxicity we all suffer ended, we would all feel so much better, have more energy, have better relationships, and have more life and positivity in everything we do. The quality of life would be orders or magnitude better than it has become under the curse of daily toxic spraying.
In fact, I have witnessed this same pattern for years. When spraying is milder during the night and next day, people are completely different; family, friends, strangers, everyone is affected. The world is a different place; a much better place. Of course, we never again experienced a night like the one I described above, where intensity dropped all the way to 3 and 4, but occasionally, intensity does drop to 7.25 during the night, and the next day, there is a noticeable difference in mood everywhere. The difference is night-and-day.
So, this is how life should be. This is the world your children and grandchildren should be growing up in. This is how it was all created to be.
I wish clear air will return again. Believe me. I have witnessed it. It changes everything.
Changing Minds: Waking People Up
Thousands of people smell and taste the poison they are injecting into the air, including myself. It is incredibly helpful for those of us who smell and/or taste it to share it with those around us. This has been one one of the most effective ways I have used to wake people up around me. Tell them when a plume hits. I tell them how good or bad the air is, and they begin to wonder if their health symptoms are quite literally modulated by the level of poison in the air at any given time. They at least begin asking the right questions.
I will warn you that people are very slow to believe it. It takes months or years of repeatedly showing someone how their health symptoms are affected by the condition of the air, but eventually, they come around. Be consistent and be persistent. People have a hard believing that something in the air which they cannot smell is affecting their life, but when you become their virtual sense of smell and taste for them, they eventually begin considering it.
My friend and business partner does not smell or taste the plumes as they hit us (unless they are exceptionally strong), however, she now knows when we are being hit and what type is hitting us. She has learned to associate certain health symptoms with certain chemtrail plume types.
After sharing with her what type is in the air over and over, and helping her correlate her aches, pains, headaches, nausea, vertigo, fatigue, etc., she now often says to me, "They are spraying the Copper type, aren't they?", or she'll say, "We're getting hit with the Mercury type, aren't we?" She has learned the association between her particular symptom-sets and particular plume types.
I am still working on friends and relatives that I only see perhaps once or twice a month. They will say, "Oh I had a horrible night's sleep.", and so I tell them how horrible the spraying was the night before. Or they will say, "The whole family is sick.", and I will say, "Well they have been spraying Biologics very strongly for the past 2 days." I will point out how interesting it is that people typically only get sick when they spray Biologic types.
So now, as I type this, it's 1:12 pm and a few minutes ago we were hit with a very strong plume, so now I'm experiencing the typical nausea, inflammation, fatigue, aches/pains, tinnitus, heart/lung issues, and other symptoms this combination of aerosolized poisons always produces.
Day-after-day, plume-after-plume... Oh how I wish people would wake up and realize that the spraying is the largest and most damaging crime against humanity in human history.
Plastics and Plastic Solvents as a Delivery System In Chemtrails
I have been reporting the strong odor of "burnt plastic" in the air since 2014. This is always combined with a solvent-like odor that resembles model-cement. I smell both the burnt plastic odor and then solvent odor as I type this.
My assertion—that you will not find in big media but is finally being hinted at in alt media—is that the primary source of these plastics is intentional aerosolization.
One critical point that neither big media or alt media has mentioned yet is the occurrence of the plastic odor and the solvent odor together. This is a huge—critical—point because model cement dissolves plastic, and so, as someone who smells and tastes this horrible material in the air, I have always believed that I have been witnessing the delivery system of aerolsolized plastic intended for human and animal exposure through inhalation:
The delivery method being that the plastic is dissolved in a solvent, then sprayed in enormous amount into the atmosphere, and then inhaled by humans and animals. This is the delivery method.
My hypothesis is that the plastic is prepared and aerosolized as a liquid in a solvent solution. When the solvent is inhaled, the body metabolizes the solvent leaving the plastic. The body then works to rid the plastics causing the symptom set we all call Morgellon's.
Practitioners know that rashes are one of the most common indicators of toxicity. As the body works to rid toxins from the body through the skin, rashes form. The polymer fibers we see in the skin rashes of Morgellon's patients may be an artifact of the plastic/polymer detoxification process.
I will be writing more on this in the future, but wanted to mention this today because Dr. Ana has released some wonderful information today about the distribution of plastics on the population and the process of dissolving them.
Much information on this subject was originally published by Dr. Hildegard Staninger many years ago. In fact, I posted this interview with Dr. Staninger in January of 2008. This information is so far ahead of the curve, that it did not receive the attention is deserves, until now.
Stay tuned.
Daily Herb Facts
Research indicates dong quai promotes oxygen absorption by the liver, raises metabolism, and enhances the liver’s ability to regulate glycogen production to normalize blood sugar levels, thus aiding in the treatment of diabetes. Dong quai has also been shown to relieve stagnation in the spleen, improve digestion, and treat constipation and dyspepsia, particularly among the elderly. Dong quai acts as a mild analgesic (pain-killer), laxative, and sedative, and exhibits some antibacterial activity against vaginal infection. Dong quai has been used to relieve pain associated with angina, arthritis, gout, injury, and neuralgia. Chinese herbalists regard dong quai as an aphrodisiac which stimulates the reproductive organs, increases the effectiveness of ovarian and testicular hormones, and enhances fertility.
Ginger contains a volatile oil and other compounds which act as digestive stimulants to encourage the production of digestive fluids and saliva. Ginger neutralizes acids and toxins in the digestive tract which reduces gas and pain in the bowel. Ginger has been shown to reduce inflammation by acting as a prostaglandin inhibitor, in much the same way as non-steroidal anti-inflammatory drugs (NSAIDs) work. Studies show ginger relaxes muscle spasms and relieves pain and inflammation associated with rheumatic conditions. Studies have found ginger produces a strong stimulating effect on muscular contractions of the heart, validating ginger’s use for improving overall circulation. According to Chinese medicine, ginger focuses its warming properties downward, toward the lower extremities, including the colon, kidneys, legs, ovaries, prostate, and vagina.
Studies show golden seal acts as an astringent, producing a vasoconstricting—tightening of the blood vessels—effect. Golden seal’s astringent ability enables it to help tone mucus membranes, which in turn, aids stomach and intestinal disorders, prostate and vaginal complaints, and stops internal bleeding and prevents hemorrhaging. Golden seal acts as a mild decongestant and laxative, relieves excess mucus, and reduces fever and inflammation associated with glandular swelling. Golden seal increases the secretion of digestive enzymes and fluids, especially bile, which helps regulate liver and spleen functions. Berberine, an isoquinoline alkaloid found in golden seal, has been studied at length in both clinical and experimental environments for its antibacterial and amebicidal properties. Furthermore, golden seal has been found to potentiate insulin and have a hypoglycemic effect which is beneficial for diabetics.
Juniper berries contain strong antiseptic, anti-inflammatory, analgesic (pain-relieving) properties which are helpful for treating infections, especially within the urinary tract. Juniper berries are an effective natural diuretic and have been found to be especially beneficial for problems of the bladder, kidneys, and prostate. Juniper berries are effective at fighting both bacterial and yeast infections, as well as chronic prostate and urinary tract infections in men with benign prostatic hypertrophy (BPH), also referred to as enlarged prostate. Juniper berries are commonly recommended for arthritis, colic, cystitis, dysuria, edema, flatulence, gout, kidney inflammation, kidney stones, poor digestion, rheumatism, sinusitis, ulcers, and urethritis. Furthermore, juniper berries are a rich source of chromium and have been used to treat blood sugar imbalances, especially diabetes.
Marshmallow is made up of about 37% starch, 11% mucilage, and 11% pectin. Marshmallow increases the production of mucosal fluids which soothes inflamed tissues and helps heal both internal and external inflammatory conditions. Marshmallow is especially beneficial for soothing and protecting mucous membranes and for counteracting excess stomach acid, gastritis, hiatal hernias, and peptic ulcers. Marshmallow is also considered mildly laxative, and is often used for various intestinal problems, including colitis, diverticulitis, enteritis, irritable bowel syndrome, and regional ileitis. As late as the mid-19th century, marshmallow was listed in the U.S. Pharmacopoeia for treating colds, diarrhea, dysentery, gastrointestinal problems, gonorrhea, hoarseness, and most any condition affecting the genito-urinary tract, including cystitis, frequent urination, incontinence, painful urination, and urinary tract infection.
Parsley stimulates production of digestive fluids and enhances the elimination of wastes from inflamed joints via the kidneys. Such action makes parsley useful for arthritis, cystitis, dyspepsia, gastritis, gout, jaundice, other liver and spleen ailments, and rheumatic conditions. Parsley helps tone the urinary system and has been used effectively for almost any type of kidney and urinary problems, including dysuria, edema, mucus in the bladder, nephritis, prostatitis, swollen breasts and glands, and urinary tract infections. Parsley also helps with stones in the bladder, gall bladder, or kidneys.
Uva ursi is an herb which focuses its many actions on the urinary system. Uva ursi soothes and tightens inflammed tissues, helps neutralize urine acidity, promotes urine flow, and acts as an antiseptic and muscle relaxant specific to the urinary tract, thus decreasing responses to pain stimuli from infections. Uva ursi also provides an anesthetic quality capable of numbing pain in the urinary system. Uva ursi has also been shown to help prevent and dissolve kidney and gallstones, induce labor, and help problems associated with diabetes and the prostate gland. Common uses include bedwetting, bladder ailments, cystitis, gonorrhea, hemorrhoids, kidney congestion and infections, nephritis, rheumatism, urinary tract infections, vaginal discharge, and venereal disease.
The Daily Spraying log
Overnight
This has been a sharp departure from the daily pattern. Are they commemorating the death of the Godfather of the New World Order... Henry Kissinger? Why are we having this sudden pattern shift?
After the onslaught of spraying/poisoning we had last night, from 3 am on we had one to the mildest nights of spraying we have had for a long time. The intensity of the air dropped to 7.25 and remained in that vicinity the entire night.
It is amazing to have quality sleep that comes with air with lower-intensity chemtrails. Chemtrails are the single largest factor in the loss of my quality of sleep.
3:01 pm
We have been hit with 3 plumes so far today. Following are the event profiles:
~6:35 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.25+, Rising
12:07 am (12/5)
Tonight we had our nightly break - a longer than usual break - from about 8 pm until 11 pm. Intensity fell to 7.5+ during this time.
The nighttime pattern was also different. We were hit at about 11 am with a mild plume that gradually increased intensity. Then at about 12 m we were hit again with another plume that pushed intensity up to the current level of 9.25.
I am so very tired of being sprayed like an insect.
12:55 am (12/5)
We have just been hit with a Burnt type plume.
~12:45 am (12/5) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.5, Rising
December 3 - The Daily Spraying Log
Don't Be Unaware: One Critical Way They Fool The Public
The long-utilized Model Cement/Burnt Plastic plume type has usually been dominant in most plumes for years. The horrific Chalky-Bitter-Pharma type is now being sprayed more intensity than most other types more often than it was just a month ago. It is moving up the dominance list more often. This is the type that produces a symptom set identical to venom peptides. For this reason, rainwater must to be sampled and tested for this. If you know of a lab that can do this, please contact me.
As someone who can acutely taste and smell the fallout from the plumes, I know they often mix the components differently. This is why I normally report the relative intensity of each component ("strongest to weakest").
Since I know the components of any single release event are mixed independently of other events, we can conclude this technology was built into the system from inception.
They knew it was critical to utilize such a system so they would have fine-grained control over the symptom set that appears in the population in a given area. They would, most certainly, design this system from the ground up to minimize "symptom clusters" on the ground. Such clusters would alert the population that "something is in the air". Imagine if everyone in your city had headaches and vertigo at the same time daily. This would be a big red flag for the public.
In a recent log entry I said that all their attacks are nearly always wrapped in psychology. This is the most important part of their system's design. They must have the ability to make the health events that they are causing appear to be "random" so the public does not catch on that they are being produced intentionally. The ability to mix components in differing proportions at will is a critical feature utilized to keep the public unaware of this historic crime against humanity.
Andrographis paniculata has been used for centuries in China, India and Thailand to successfully treat upper respiratory tract infection, fever and sore throat, as well as other infectious and chronic diseases. Andrographis is also used extensively in Scandinavian countries to prevent and treat common colds and flu. Andrographis is used therapeutically for bacterial and viral respiratory infections including common cold, pharyngotonsillitis (inflammation of the pharynx and tonsils) and acute sinusitis; as a prophylactic (preventative measure) for the common cold; to boost immune function in bacterial and viral infections; and to relieve fever. Andrographis does not appear to work as an antiviral or antibacterial agent directly, but rather as a potent stimulator of the immune response. Researchers have confirmed that andrographolide, the major constituent, demonstrates immunostimulatory activity as evidenced by increased proliferation of lymphocytes (white blood cells that fight infection and disease) and production of interleukin-2 (a substance that stimulates the growth of certain disease-fighting blood cells in the immune system). Such activity contributes to the effectiveness of andrographis in the prevention and treatment of uncomplicated acute upper respiratory tract infections such as the common cold. For example, a randomized, double-blind trial involving 158 patients with the common cold found that andrographis produced a significant decrease in the prevalence and intensity of cold symptoms (i.e. nasal secretions, sore throat, sleeplessness, tiredness) as early as the second day of treatment compared to placebo. Furthermore, a randomized, double blind, placebo-controlled clinical trial showed a significant decrease in the incidence of colds in school children given an andrographis extract for 3 months during the winter season. Generally there are few side effects associated with the use of andrographis, and it has extremely low toxicity. However, the antifertility effect demonstrated in female mice (although high doses were used) suggests that andrographis should not be used by women who wish to become pregnant or during pregnancy, especially in the first trimester.1-9
Thyme acts as an antibacterial agent, antitussive, expectorant and bronchial antispasmodic (a substance that relaxes bronchial spasms). Thyme also provides analgesic (pain-relieving) and diaphoretic (increases perspiration to lower fever) activity. Commonly recommended for bronchitis and coughs, thyme is also used in the treatment of inflamed sinuses, nose and throat, and as a natural remedy for asthma, laryngitis and whooping cough. Thyme contains volatile oils that provide antimicrobial and anti-inflammatory benefits in upper respiratory infections. Thymol, the principal active ingredient, combats bronchial spasms, inhibits the growth of bacteria, and helps loosen phlegm. Thyme is approved by the German Commission E for bronchitis, whooping cough and upper respiratory inflammation; however, its use is not recommended during pregnancy.10-16
Bitter orange fruit (Fructus aurantia) is commonly used as an expectorant for eliminating excess phlegm and relieving congestion. Research indicates that bitter orange contains the flavone nobiletin, a potent antioxidant that exhibits anti-allergic, antihistaminic and anti-inflammatory actions. In addition, bitter orange contains the active ingredient synephrine, which provides decongestant effects on the respiratory system. Synephrine helps maintain normal blood pressure levels, while simultaneously providing decongestant effects such as increasing circulation to the head, shrinking swollen tissues, and dilating respiratory passages to improve breathing. Such evidence helps support the use of bitter orange in herbal nasal decongestants, and lends credence to its use for allergies, asthma, coughs and symptoms associated with colds. Furthermore, researchers studied 34 kinds of traditional herbal medicines and found that bitter orange fruit had the most potent inhibitory activity on rotavirus infection—rotavirus may be the most important cause of severe dehydrating diarrhea in children under 3 years of age.17-25
Eleuthero, commonly known as Siberian ginseng, has demonstrated antioxidant and immuno-enhancing effects. Researchers have identified 6 compounds in eleuthero that show various levels of activity as antioxidants, while 4 compounds exhibit anticancer actions and 2 show immunostimulatory effects. An in vitro study found that an eleuthero preparation increased phagocytosis—the ingestion of waste material, harmful microorganisms or other foreign bodies—of Candida albicans by granulocytes and monocytes (types of white blood cells) from healthy donors by 30-45%. Likewise, a liquid eleuthero root extract demonstrated strong antiviral activity and inhibited the replication of human rhinovirus (one of the major causes of the common cold), respiratory syncytial virus (a major cause of respiratory illness), and influenza A (flu) virus in infected cell cultures. Furthermore, a double-blind, placebo-controlled German study involving 36 healthy volunteers demonstrated that eleuthero boosts immune system response and enhances the body's overall resistance to infection, as evidence by a dramatic increase in the total number of lymphocytes (white blood cells that fight infection and disease), especially T-lymphocytes.15,26-38
Oregano has been used as a folk medicine for centuries for diarrhea, fevers, headaches and respiratory disorders such as bronchitis, colds and coughs. Oregano contains the active ingredients carvacrol and thymol, which provide antimicrobial and anti-inflammatory benefits in upper respiratory infections, as well as help loosen phlegm in the lungs and relieve spasms in the bronchial passages. Research on the biological activity of oregano has confirmed a wide range of antibacterial, antifungicidal, antiviral, antioxidant and expectorant properties, both for the essential oil, as well as the extracts, including inhibitory activity against Klebsiella pneumoniae—a cause of respiratory infections. In fact, the essential oil of oregano is recommended for treatment of acute bacterial infections of the bronchi and may provide relief through inhalation by individuals with chronic asthma, combined with bronchitis.11,39-42
References: 1Barilla MS, J. "Andrographis paniculata." Better Nutrition; June 1999. 2Friedland, J. "Is Andrographis The Next Big Immune Booster?" Natural Foods Merchandiser; August 2001. 3Lukaczer ND, D. "Nutrition Q&A with Dan Lukaczer, N.D." Natural Foods Merchandiser; February 2003. 4Lenz, E. "Andrographis." Gale Encyclopedia of Alternative Medicine. cf_dls/g2603/0001/2603000154/p1/article.jhtml>. Accessed March 2004. 5Bone, K. "Andrographis for colds and sinus infection." Townsend Letter for Doctors and Patients; January 2003. 6Puri, A., et. al. "Immunostimulant agents from Andrographis paniculata." Journal of Natural Products; 1993, 56(7):995-999. 7Rajagopal, S., et. al. "Andrographolide, a potential cancer therapeutic agent isolated from Andrographis paniculata." Journal of Experimental Therapeutics & Oncology; 2003, 3(3):147-158. 8Poolsup, N., et. al. "Andrographis paniculata in the symptomatic treatment of uncomplicated upper respiratory tract infection: systematic review of randomized controlled trials." Journal of Clinical Pharmacy and Therapeutics; 2004, 29(1):37-45. 9Caceres, D.D., et. al. "Use of visual analogue scale measurements (VAS) to asses the effectiveness of standardized Andrographis paniculata extract SHA-10 in reducing the symptoms of common cold. A randomized double blind-placebo study." Phytomedicine.; 1999, 6(4):217-223. 10Broadhurst PhD, C.L. "Natural Asthma Relief." Nutrition Science News; April 1999. 11White MD, L.B. "Soothing Children's Sore Throats Naturally." Nutrition Science News; April 2000. 12"Thyme." PDRhealth, 2003. . Accessed March 2004. 13PDR for Herbal Medicines, 2nd Ed. Montvale, NJ: Medical Economics Company, 2000. 14Hanrahan, C. "Thyme." Gale Encyclopedia of Alternative Medicine. cf_dls/g2603/0007/2603000704/p1/article.jhtml>. Accessed March 2004. 15Fetrow PharmD, C. & Avila PharmD, J. Professional’s Handbook of Complementary & Alternative Medicines. Springhouse, PA: Springhouse Corp., 1999. 16Herbal Medicine: Expanded Commission E Monographs. Newton, MA: Integrative Medicine Comm., 2000. 17Bensky, D. & Gamble, A. Chinese Herbal Medicine Materia Medica, Revised Edition. Eastland Press, 2003. 18Ody, P. The Complete Medicinal Herbal. NY, NY: Dorling Kindersley, Inc., 1993. 19Mindell PhD, E. Earl Mindell’s Supplement Bible. NY, NY: Fireside, 1998. 20Duke PhD, J. "Nobiletin."Dr. Duke’s Phytochemical and Ethnobotanical Databases. . Accessed March 2004. 21Takase, H., et. al. "Pharmacological profile of gastric mucosal protection by marmin and nobiletin from a traditional herbal medicine, Aurantii fructus immaturus." Japanese Journal of Pharmacology; 1994, 66(1): 139-147. 22Murakami, A., et. al. "Suppressive effects of citrus fruits on free radical generation and nobiletin, an anti-inflammatory polymethoxyflavonoid." Biofactors; 2000, 12(1-4): 187-192. 23Urdang, L. & Swallow, H. H. (Eds.). Mosby’s Medical & Nursing Dictionary. St. Louis, MO: The C. V. Mosby Company, 1983. 24Huang, Y.T., et. al. "Fructus aurantiireduced portal pressure in portal hypertensive rats. Life Sciences; 1995, 57(22): 2011-2020. 25Kim, D.H., et. al. "Inhibitory effect of herbal medicines on rotavirus infectivity." Biological & Pharmaceutical Bulletin; 2000, 23(3):356-358. 26Lininger DC, S., et al. The Natural Pharmacy, 2nd ed. Rocklin, CA: Prima Health, 1999. 27Pizzorno, J. & Murray, M. Textbook of Natural Medicine, 2nd ed. London: Churchill Livingstone, 1999. 28Vukovic, L. "Get Ready for the Cold and Flu Season." Natural Foods Merchandiser; October 2003. 29Davydov, M. & Krikorian, A.D. "Eleutherococcus senticosus (Rupr. & Maxim.) Maxim. (Araliaceae) as an adaptogen: a closer look." Journal of Ethnopharmacology; 2000, 72(3):345-393. 30Deyama, T., et. al. "Constituents and pharmacological effects of Eucommia and Siberian ginseng." Acta Pharmacologica Sinica; 2001, 22(12):1057-1070. 31"Radix Eleutherococci." In: WHO monographs on selected medicine plants, Volume 2. Geneva, Switzerland: World Health Organization. trm/medicinalplants/vol2/083to096.pdf>. Accessed December 2003. 32Bol'shakova, I.V., et. al. [Antioxidant properties of a series of extracts from medicinal plants]. Biofizika; 1997, 42(2):480-483. 33Wildfeuer, A. & Mayerhofer, D. [The effects of plant preparations on cellular functions in body defense]. Arzneimittelforschung; 1994, 44(3):361-366. 34Glatthaar-Saalmuller, B., et. al. "Antiviral activity of an extract derived from roots of Eleutherococcus senticosus." Antiviral Research; 2001, 50(3):223-228. 35"Antibody-mediated neutralization of human rhinovirus 14." http://bilbo.bio.purdue.edu/~viruswww/ Smith_home/HRV14Fab/HRV14Fab.html>. Accessed December 2003. 36Leshin MD, L. "Respiratory Syncytial Virus (RSV)." Down Syndrome: Health Issues, 2001. . Accessed December 2003. 37Bohn, B., et. al. "Flow-cytometric studies with eleutherococcus senticosus extract as an immunomodulatory agent." Arzneimittelforschung; 1987, 37(10):1193-1196. 38Newall, C., et. al. Herbal Medicines. London: The Pharmaceutical Press, 1996. 39"Oregano." PDRhealth, 2003. . Accessed March 2004. 40Foster, S. "The fighting power of Oregano: this versatile herb packs a powerful punch." Better Nutrition; March 2002. 41Hammer KA, et. al. "Antimicrobial activity of essential oils and other plant extracts." Journal of Applied Microbiology; 1999, 86(6):985-990. 42Schnaubelt PhD, K. Advanced Aromatherapy. Rochester, VT: Healing Arts Press, 1995.
The Daily Spraying Log
The last major hit we had last night was at 2:36 am. It is normal for them to hit us this far into the morning over the past several months.
This morning, air was at near-ambient intensity all morning until 11:20 am. Intensity remained at about 7.75 with the typical wide-spectrum mix of poisons which include agents that induce heart, lung, and arterial inflammatory. What a time we live in.
The lull in spraying this morning before 11:20 am is likely due to the incoming snow storm that will drop 3 to 5 inches on us. They are likely "working" that storm so their assets (jets) are tied up there.
4:15 pm
Now, as expected, we have been hit hard and they are layering the air to keep plume fallout intensity high, and boy is it high.
Following are the event profiles for the day so far:
I cannot express how tired I am of being poisoned like this. Absolutely no words.
~11:20 pm Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.5+, Rising
1:47 am (12/4)
Here we go again. Another horrible plume. This is one of the light plumes that I call a "layering" plume. It only raised intensity to 8.25+, which is still bad, but less intense than usual.
~2:25 am (12/4) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.5-, Rising
December 2 - The Daily Spraying Log
The overnight report is simple. They hit us with plumes at 2-hour intervals: 6:30 am, 8:30 am, 10:30 am. As I'm typing this, they hit us again, at 12:30 pm. They used the same 2-hour interval yesterday afternoon.
They used the same wide-spectrum plumes all night. The dominant plumes were the Chalky-Bitter-Pharma and Inflammatory types. These 2 plumes are now being used as dominant more often than ever before.
They cause numerous issues including arterial inflammation, heart inflammation, lung inflammation, head pressure, fatigue, and more. Click the plume type-name to learn details about these plume types. You may find that your symptoms are included in the symptoms these poisons cause.
Following is the current event profile. They used the identical plume profile throughout the night:
Tonight, they are following the same schedule they do on most nights. At about 10:20 pm they hit us with a mildish plume, then just before 11 pm they hit us with a strong plume.
These 2 plumes have different component profiles; same components but different potencies.
Following are the event profiles:
~10:18 pm Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Chalky-Bitter-Pharma - Inflammatory - Stimulant - This is the newest type. - Model Cement/Burnt Plastic - See Microplastics - Mercury Intensity Delta: Medium-Fast Peak Intensity: 8.25 - This is like a "layering" plume; a plume used to maintain the intensity of previous plumes.
So here is an interesting pattern. We had a "break" from about 11:30 pm until 1:10 am (12/3). Intensity dropped to 7.25 and it was wonderful to have all of my health symptoms disappear for a little while.
Since the last log entry, we have been hit with 2 more plumes.
~1:10 am (12/3) Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Chalky-Bitter-Pharma - Inflammatory - Stimulant - This is the newest type. - Model Cement/Burnt Plastic - See Microplastics - Mercury Intensity Delta: Medium-Fast Peak Intensity: 8+ - This is like a "layering" plume; a plume used to maintain the intensity of previous plumes.
Notice the parallel between the 10:18 and 10:47 pm plumes and the 1:10 and 1:41 am plumes. It's as if the 2 events at 10:18 and 10:47 pm repeated themselves at 1:10 and 1:41 am.
The component ratios (strongest to weakest) were the same, plus the first plume in each group was a milder, "layering" plume, and the second was an intense plume with the Model Cement/Burnt Plastic type being dominant.
Interesting.
Intensity is now 9.5 in just the time it took me to proof read this and post it.
The attack on all life continues.
2:36 am (12/3)
We have just been hit with a Burnt type plume. It was very strong but passed very quickly.
~2:25 am (12/3) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Peak Intensity: 9.25
December 1- Yes! They are Spraying You With Microplastics
Since 2014, we have been reporting the strong odor of solvents and plastics in chemtrails:
In the October 2023 Daily Spraying Log, I reported the spraying of extremely-intense plastic-type chemtrails causing numerous people to smell and taste them in the air. Media was blaming the odor on the Canadian fires, but this is a lie. The odor was identical to the plastic chemtrail type they have sprayed since before 2014. This overwhelming plastic odor was accompanied by an equally-intense odor of model cement. These two odors have always been used together since I began reporting them in 2014.
The October Spraying Log - Search the page for the word "fire". You can search by pressing Ctrl-F.
For years, we have reported the presence of microplastics in the atmosphere, even posting mainstream articles talking about it. Of course, they blame this unbelievable amount of plastic "pollution" on the public, but that is another lie. The real source is chemical aerosol injection:
And now, we have a new interview with Dr. Ana Mihalcea presenting laboratory evidence that these plastics are being found, not only in the air, but in vaccines, mRNA injections, and even in dental anesthetics:
Microplastics Found In Air, mRNA Jabs, and Dental Anesthetics
The aroma of peppermint oil is extremely refreshing, with the ability to clear the head, increase mental clarity and alertness, and sharpen the senses. Peppermint oil is also beneficial for reviving individuals following episodes of dizziness, fainting, nausea or even shock. Psychologically, peppermint can lift one’s mood out of a state of boredom or emotional fatigue.1-3
Peppermint oil’s analgesic (pain-relieving) and antispasmodic properties help relieve headache and sinus pain, muscle aches, neuralgia, toothache, and menstrual discomfort. Peppermint oil’s analgesic effects may also be helpful for relieving the pain associated with rheumatoid arthritis.4
Applied topically, peppermint oil causes local blood vessels to dilate, which produces a cooling effect that is beneficial for bringing down a fever, treating sunburn, or easing hot flashes. Animal studies have shown that the topical application of 1-2 drops of peppermint oil directly on the temples produces this cooling effect by altering calcium channels of the body’s cold receptors. Animal studies have also confirmed that peppermint oil is responsible for restricting serotonin and substance P (neurotransmitters that carry pain messages to the brain) in smooth muscle contraction, and for increasing circulation in the skin.1,4,5
German scientists took this research a step further by conducting a randomized double-blind, placebo-controlled clinical study to determine the effects of essential oils for relieving headaches. Study results showed that when a peppermint and eucalyptus oil preparation was applied topically to large areas of the forehead and temples, it increased cognitive performance and produced a muscle-relaxing and mentally relaxing effect. However, when researchers applied a preparation of peppermint oil alone, it provided significant analgesic effects, causing the greatest decrease in the participants’ sensitivity to headache pain. Incidentally, both essential oils are well-recognized transmitters in the trigemino-vascular system, which is the leading structure in the generation of primary headaches.6-8
A follow-up study to determine the effects of topical application on different types of experimentally-induced headache pain (ischemically-induced headache, thermal pain induction, experimentally-induced pain, etc.) again confirmed that peppermint oil provides significant analgesic effects. Researchers concluded that topical use of peppermint and eucalyptus oils may prove to be an effective and simple alternative therapy for the treatment of headaches, and one that is free of the potential side-effects associated with analgesics such as acetaminophen and aspirin.8,9
Peppermint oil is an antiseptic and decongestant, especially effective as an inhalant for respiratory conditions, including colds, flu and general malaise.1
Researchers in India have confirmed that peppermint essential oil acts as a bactericide against Escherichia coli (E. coli) strain SP-11. A follow-up study of broader scope determined that peppermint oil is also effective as an antibacterial and antifungal against at least 22 Gram-positive and Gram-negative bacteria and 11 yeast-like and filamentous fungi in vitro. In fact, peppermint oil was found to be among the most potent of botanical oils tested against anaerobic oral bacterial. Furthermore, a peppermint oil preparation was tested in vitro against headlice (Pediculus humanus capitis) and found to be an effective treatment.10-13
According to recent research, the essential oils of Mentha piperita, Citrus limon, and Eucalyptus globulus have been analyzed and found to be effective antibacterial agents against methicillin-resistant Staphylococcus aureus (MRSA). This antibiotic-resistant strain has been responsible for the rapid spread of infectious outbreaks around the world. In fact, a mutated form of MRSA was determined as the cause of the “flesh-eating bug” of 1994.4
Researchers from Minia University in Egypt tested various essential oils to determine their inhibitory effects on dermatophytic fungi—any of several fungi that cause parasitic skin disease in humans. Results showed that clove and peppermint oils provided strong fungistatic effects, seriously inhibiting the growth of tested fungi. Such impressive results prompted researchers to suggest adding clove and peppermint oils in antidermatophytic drugs.14
According to an article published in the International Journal of Aromatherapy, essential oils are used to enhance the quality of life of Alzheimer’s patients. For example, the essential oils of geranium and lavender are used to trigger memories of cooking and plants, while eucalyptus, peppermint and pine oils are used to stimulate conversation and overall memory.4
Inhaling peppermint (Mentha piperita) oil may help reduce nausea associated with chemotherapy and radiation treatments. Inhaling the scent of peppermint essential oil has also been shown to reduce peripheral blood pressure.4,5
Peppermint oil is contraindicated for individuals with epilepsy or insomnia, and should not be used topically on children under 3 years of age. Peppermint oil should also be applied sparingly on those with sensitive skin, in order to avoid minor skin irritation. Furthermore, since peppermint oil promotes menstruation and reduces lactation, its use is best avoided during the first trimester of pregnancy and while nursing.2-4,15
NSP's Peppermint oil is 100% pure Mentha piperita leaf and flower oil.
References: 1Damian, P. and Damian, K. Aromatherapy: Scent and Psyche. Rochester, VT: Healing Arts Press, 1995. 2Wildwood, C. The Encyclopedia of Aromatherapy. Rochester, VT: Healing Arts Press, 1996. 3Schiller, C. and Schiller, D. Aromatherapy Oils: A Complete Guide. NY, NY: Sterling Publishing Co., 1996. 4Buckle RGN, J. Clinical Aromatherapy in Nursing. San Diego, CA: Singular Publishing Co., 1997. 5Tucker PhD, A. “The therapy of aroma.” Herbs For Health; 1999, 3(6): 46-50. 6Göbel, H., et. al. “Effect of peppermint and eucalyptus oil preparations on neurophysiological and experimental algesimetric headache parameters.” Cephalalgia; 1994, 14(3): 228-234. 7McCaleb, R. “Essential Oils For Fast Relief Of Headache Pain.” HerbalGram; 1995, No. 35. 8Brown ND, D. “Essential Oils For Headache Treatment.” HerbalGram; 1998, No. 38. 9Göbel, H., et. al. “Essential plant oils and headache mechanisms.” Phytomedicine; 2(2): 93-102. 10Pattnaik, S., et. al. “Effect of essential oils on the viability and morphology of Escherichia coli.” Microbios; 1995, 84(340): 195-199. 11—. “Antibacterial and antifungal activity of ten essential oils in vitro.” Microbios; 1996, 86(349): 237-246. 12Shapiro, S., et. al. “The antimicrobial activity of essential oils and essential oil components towards oral bacteria.” Oral Microbiol Immunol; 1994, 9(4): 202-208. 13Veal, L. “The potential effectiveness of essential oils as a treatment for headlice, Pediculus humanus capitis.” Complementary Therapies in Nursing and Midwifery; 1996, 2(4): 97-101. 14el-Naghy, M.A., et. al. “Fungistatic action of natural oils and fatty acids on dermatophytic and saprophytic fungi.” Zentralbl Mikrobiol; 1992, 147(3-4): 214-220. 15Schnaubelt PhD, K. Advanced Aromatherapy. Rochester, VT: Healing Arts Press, 1995.
Since they hit us at about 9:30 am, they have been laying to keep intensity at 9.75, which is unbearable for sensitive persons.
Following is the event profile for the 9:30 am drop:
~9:30 am Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Model Cement/Burnt Plastic - Dominant, This is very strong. See Microplastics Found In mRNA Jabs and Dental Anesthetics - Chalky-Bitter-Pharma - This is also very strong. - Inflammatory - They are using a new inflammatory mix that appears to target the brain and heart. This is brutal for those predisposed to inflammation. - Stimulant - Mercury Intensity Delta: Medium-Fast Current Intensity: 9.75
The assault on all life continues.
12:02 pm
They have been layering the previous plume keeping intensity high without any breaks. Intensity is still 9.75 as I type this.
12:22 pm
The previous wide-spectrum plume is still being layered and is currently at intensity 9.75-.
We have just been hit with a Burn type plume:
~12:20 am (12/1) Event: Hit with single-component plume Type: Burnt Electronics/Fungal Intensity Delta: Fast Current Intensity: 9.25, Rising
11:44 pm
This afternoon has been interesting; a departure from recent spray patterns.
Recently, they layered the air all afternoon at a high intensity. Today, we were hit with plumes roughly every 2 hours. Intensity dropped to 7.5+ to 7.75 between plumes. Plumes were not direct hits, and they were not layered. They were the same type they have used during the afternoon for days.
Peak intensity of all plumes were between 8.75 and 9.25 and consisted of the following components:
- Model Cement/Burnt Plastic - Dominant, This is very strong. See Microplastics Found In mRNA Jabs and Dental Anesthetics - Chalky-Bitter-Pharma - This is also very strong. - Inflammatory - They are using a new inflammatory mix that appears to target the brain and heart. This is brutal for those predisposed to inflammation. - Stimulant - Mercury
I don't know why today's pattern was so different, but at least it was less intense overall than recent days.
We'll have to see what happens next.
1:35 am (12/2)
Well, this is what happens next.
We have been hit with a strong plume at about 1:20 am. This is a common nighttime time for us to be hit.
Following is the event profile:
1:20 am (12/2) Event: Hit with wide-spectrum plume. Components (strongest to weakest): - Inflammatory - This is very potent in this plume. - Model Cement/Burnt Plastic - This is also very strong. - Chalky-Bitter-Pharma - Stimulant - Mercury Intensity Delta: Medium-Fast Current Intensity: 9.25, Rising
Last edited by Russ Tanner; 01/01/2406:53 AM.
Russ Tanner, Founder, Administrator, Programmer GlobalSkywatch.com My Chemtrail Story
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